Human (GRCh38.p14)
Description

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

Gene Synonyms

AS

Location

Scaffold HSCHR6_MHC_MANN_CTG1: 2,578,541-2,665,857 reverse strand.

GRCh38:GL000253.2

View this gene on the primary assembly.

About this gene

This gene has 10 transcripts (splice variants), 1 gene allele and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000435618.6HLA-B-2211605362aaENSP00000405178.2
 
Protein coding
Q2L6G2 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000436729.5HLA-B-2221154241aaENSP00000403471.1
 
Protein coding
A0A140T9H3 -TSL:NACDS 5' incomplete
ENST00000430299.1HLA-B-220820246aaENSP00000416672.1
 
Protein coding
A0A140T9Y5 -TSL:NACDS 3' incomplete
ENST00000639633.1HLA-B-22824080aaENSP00000492667.1
 
Protein coding
A0A1W2PQE2 -GENCODE basicTSL:NA
ENST00000640538.1HLA-B-22914749aaENSP00000491837.1
 
Protein coding
A0A1W2PP67 -GENCODE basicTSL:NA
ENST00000481283.5HLA-B-2241008224aaENSP00000435817.1
 
Nonsense mediated decay
A0A140TA14 -TSL:NA
ENST00000489762.1HLA-B-2261085No protein-
 
Retained intron
--TSL:NA
ENST00000488367.5HLA-B-225917No protein-
 
Retained intron
--TSL:NA
ENST00000492573.5HLA-B-227753No protein-
 
Retained intron
--TSL:NA
ENST00000465455.1HLA-B-223588No protein-
 
Retained intron
--TSL:NA