Human (GRCh38.p14)
Description

apolipoprotein B [Source:HGNC Symbol;Acc:HGNC:603]

Location

Chromosome 2: 21,001,429-21,044,073 reverse strand.

GRCh38:CM000664.2

View alleles of this gene on alternative sequences

About this gene

This gene has 4 transcripts (splice variants), 1 gene allele, 355 orthologues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000233242.5APOB-201141214563aaENSP00000233242.1
 
Protein coding
CCDS1703P04114 NM_000384.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399256.4APOB-2023128828aaENSP00000382200.4
 
Protein coding
A8MUN2 -GENCODE basicTSL:1
ENST00000673739.2APOB-2035489179aaENSP00000501110.2
 
Nonsense mediated decay
A0A669KB70 --
ENST00000673882.2APOB-2043840179aaENSP00000501253.2
 
Nonsense mediated decay
A0A669KB70 --