What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 75892-0: t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points Molgen Nom (Bld/Tiss)

Name: LOINC Code 75892-0: t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points Molgen Nom (Bld/Tiss)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T08:59:56.385Z

75892-0 is a LOINC code used to identify t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points Molgen Nom (Bld/Tiss) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points. It is commonly used with the system or sample type Bld/Tiss.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points. It is commonly used with the system or sample type Bld/Tiss.

When is it used?

Used in lab systems, EHRs, and clinical data exchange.
May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
Status: ACTIVE
Order vs observation: Both
Method: Molgen

What it does not mean

The code identifies the observation or test, not the actual result.

Key facts

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points [Identifier] in Blood or Tissue by Molecular genetics method Nominal
t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points
Used to report the major (p210), minor (p190), and micro (p230) BCR-ABL1 breakpoints, which together account for the vast majority of BCR-ABL1 gene fusion events in CML and ALL.
ABL; ALL; bcr/abl; BCR1; bcr-abl1; Blood; break pts; breakpoint; Breakpoint cluster region; Chronic myeloid leukemia; CML; D22S11; D22S662; DNA; gene fusion; gene translocation; Genetics; Heredity; Heritable; Identity or presence; Inherited; JTK7; major breakpoints; Mbr; Mcr; minor breakpoints; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; Nominal; p150; PCR; Ph chromosome; Philadelphia chromosome; PHL; Point in time; Random; RNA; T prime; t(9,22)(ABL1,BCR) gene translocation; t(9,22)(ABL1,BCR) Translocation; t(9,22)(q34,q11); t(9,22)(q34.1,q11); t(9;22)(ABL1,BCR); Tissue; Tissue, unspecified; translocation; v-abl Abelson murine leukemia viral oncogene homolog 1; WB; Whole blood; Whole blood or Tissue

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points Molgen Nom (Bld/Tiss)t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points [Identifier] in Blood or Tissue by Molecular genetics method Nominalt(9;22)(ABL1,BCR) break pts Bld/Tt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break pointsMOLPATH.TRNLOCt(9;22)(q34.1;q11)(ABL1,BCR) break point analysis, Blood or tissue specimenPrid

Frequently asked questions

Code details

Code75892-0

SystemLOINC

Display namet(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points Molgen Nom (Bld/Tiss)

Descriptiont(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points

Short namet(9;22)(ABL1,BCR) break pts Bld/T

Componentt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points

PropertyPrid

TimingPt

System (specimen)Bld/Tiss

ScaleNom

MethodMolgen

ClassMOLPATH.TRNLOC

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.50

Last changed2.50

Consumer names

t(9;22)(q34.1;q11)(ABL1,BCR) break point analysis, Blood or tissue specimen

Part names

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break pointsPridPtBld/TissNomMolgenPresence or IdentityPoint in time (spot)Blood or TissueMolecular genetics

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.