Canonical Allele Identifier: CA136831435

Gene: HLA-B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354270A>T , CM000668.2:g.31354270A>T	GRCh38
NC_000006.11:g.31322047A>T , CM000668.1:g.31322047A>T	GRCh37
NC_000006.10:g.31430026A>T	NCBI36
NG_023187.1:g.7943T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3167T>A
ENST00000481849.6:n.3127T>A
ENST00000497377.6:n.3034T>A
ENST00000696558.1:c.1189T>A	ENSP00000512716.1:n.1189T>A
ENST00000696559.1:c.*31T>A	ENSP00000512717.1:n.*31T>A
ENST00000696560.1:c.*31T>A	ENSP00000512718.1:n.*31T>A
ENST00000696561.1:c.*31T>A	ENSP00000512719.1:n.*31T>A
ENST00000696562.1:c.*31T>A	ENSP00000512720.1:n.*31T>A
ENST00000412585.7:c.*31T>A MANE Select	ENSP00000399168.2:n.*31T>A
ENST00000412585.6:c.*31T>A	ENSP00000399168.2:n.*31T>A
ENST00000481849.5:n.355T>A
ENST00000497377.5:n.519T>A
NM_005514.6:c.*31T>A	NP_005505.2:n.*31T>A
XM_011514556.1:c.*31T>A	XP_011512858.1:n.*31T>A
XM_011514557.1:c.*31T>A	XP_011512859.1:n.*31T>A
XR_926175.1:n.1559T>A
NM_005514.7:c.*31T>A	NP_005505.2:n.*31T>A
NM_005514.8:c.*31T>A MANE Select	NP_005505.2:n.*31T>A