Canonical Allele Identifier: CA136831541

Gene: HLA-B

Linked Data

• dbSNP Id: rs2428494
• gnomAD v2: 6-31322197-T-A
• gnomAD v3: 6-31354420-T-A
• gnomAD v4: 6-31354420-T-A
• MyVariant Identifiers: chr6:g.31322197T>A (hg19) ; chr6:g.31354420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354420T>A , CM000668.2:g.31354420T>A	GRCh38
NC_000006.11:g.31322197T>A , CM000668.1:g.31322197T>A	GRCh37
NC_000006.10:g.31430176T>A	NCBI36
NG_023187.1:g.7793A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3140+59A>T
ENST00000481849.6:n.3100+59A>T
ENST00000497377.6:n.3007+59A>T
ENST00000696558.1:c.1162+59A>T	ENSP00000512716.1:n.1162+59A>T
ENST00000696559.1:c.*4+59A>T	ENSP00000512717.1:n.*4+59A>T
ENST00000696560.1:c.*4+59A>T	ENSP00000512718.1:n.*4+59A>T
ENST00000696561.1:c.*4+59A>T	ENSP00000512719.1:n.*4+59A>T
ENST00000696562.1:c.*4+59A>T	ENSP00000512720.1:n.*4+59A>T
ENST00000412585.7:c.*4+59A>T MANE Select	ENSP00000399168.2:n.*4+59A>T
ENST00000412585.6:c.*4+59A>T	ENSP00000399168.2:n.*4+59A>T
ENST00000481849.5:n.328+59A>T
ENST00000497377.5:n.492+59A>T
NM_005514.6:c.*4+59A>T	NP_005505.2:n.*4+59A>T
XM_011514556.1:c.*4+59A>T	XP_011512858.1:n.*4+59A>T
XM_011514557.1:c.*4+59A>T	XP_011512859.1:n.*4+59A>T
XR_926175.1:n.1532+59A>T
NM_005514.7:c.*4+59A>T	NP_005505.2:n.*4+59A>T
NM_005514.8:c.*4+59A>T MANE Select	NP_005505.2:n.*4+59A>T