Canonical Allele Identifier: CA1087465790

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355611-A-C
• gnomAD v4: 6-31355611-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355611A>C , CM000668.2:g.31355611A>C	GRCh38
NC_000006.11:g.31323388A>C , CM000668.1:g.31323388A>C	GRCh37
NC_000006.10:g.31431367A>C	NCBI36
NG_023187.1:g.6602T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2648T>G
ENST00000481849.6:n.2093-19T>G
ENST00000497377.6:n.2093-19T>G
ENST00000640094.2:c.620-19T>G	ENSP00000491275.2:n.620-19T>G
ENST00000696558.1:c.689-19T>G	ENSP00000512716.1:n.689-19T>G
ENST00000696559.1:c.620-19T>G	ENSP00000512717.1:n.620-19T>G
ENST00000696560.1:c.620-19T>G	ENSP00000512718.1:n.620-19T>G
ENST00000696561.1:c.620-19T>G	ENSP00000512719.1:n.620-19T>G
ENST00000696562.1:c.620-19T>G	ENSP00000512720.1:n.620-19T>G
ENST00000412585.7:c.620-19T>G MANE Select	ENSP00000399168.2:n.620-19T>G
ENST00000412585.6:c.620-19T>G	ENSP00000399168.2:n.620-19T>G
ENST00000434333.1:c.653-19T>G	ENSP00000405931.1:n.653-19T>G
ENST00000463574.1:n.192T>G
ENST00000474381.1:n.1050T>G
ENST00000498007.1:n.886-19T>G
NM_005514.6:c.620-19T>G	NP_005505.2:n.620-19T>G
XM_011514556.1:c.653-19T>G	XP_011512858.1:n.653-19T>G
XM_011514557.1:c.620-19T>G	XP_011512859.1:n.620-19T>G
XR_926175.1:n.1059-19T>G
NM_005514.7:c.620-19T>G	NP_005505.2:n.620-19T>G
NM_005514.8:c.620-19T>G MANE Select	NP_005505.2:n.620-19T>G