Human (GRCh38.p14)
Description

major histocompatibility complex, class I, B [Source:HGNC Symbol;Acc:HGNC:4932]

Gene Synonyms

AS

Location

Scaffold HSCHR6_MHC_COX_CTG1: 2,750,417-2,837,604 reverse strand.

GRCh38:GL000251.2

View this gene on the primary assembly.

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000425848.6HLA-B-2121605362aaENSP00000400842.2
 
Protein coding
Q5SS57 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000416726.5HLA-B-2111154241aaENSP00000392099.1
 
Protein coding
A0A140T951 -TSL:NACDS 5' incomplete
ENST00000445222.1HLA-B-213863246aaENSP00000399675.1
 
Protein coding
A0A140T9D4 -TSL:NACDS 3' incomplete
ENST00000640223.1HLA-B-21924080aaENSP00000491916.1
 
Protein coding
A0A1W2PQE2 -GENCODE basicTSL:NA
ENST00000461583.5HLA-B-2141008224aaENSP00000436637.1
 
Nonsense mediated decay
A0A140TA21 -TSL:NA
ENST00000470915.1HLA-B-2151088No protein-
 
Retained intron
--TSL:NA
ENST00000473379.5HLA-B-217917No protein-
 
Retained intron
--TSL:NA
ENST00000472294.5HLA-B-216753No protein-
 
Retained intron
--TSL:NA
ENST00000490676.1HLA-B-218586No protein-
 
Retained intron
--TSL:NA