Canonical Allele Identifier: CA2677952719

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31353911-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353911T>C , CM000668.2:g.31353911T>C	GRCh38
NC_000006.11:g.31321688T>C , CM000668.1:g.31321688T>C	GRCh37
NC_000006.10:g.31429667T>C	NCBI36
NG_023187.1:g.8302A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3526A>G
ENST00000481849.6:n.3486A>G
ENST00000497377.6:n.3393A>G
ENST00000696558.1:c.1548A>G	ENSP00000512716.1:n.1548A>G
ENST00000696559.1:c.*390A>G	ENSP00000512717.1:n.*390A>G
ENST00000696560.1:c.*390A>G	ENSP00000512718.1:n.*390A>G
ENST00000696561.1:c.*390A>G	ENSP00000512719.1:n.*390A>G
ENST00000696562.1:c.*390A>G	ENSP00000512720.1:n.*390A>G
ENST00000412585.7:c.*390A>G MANE Select	ENSP00000399168.2:n.*390A>G
ENST00000412585.6:c.*390A>G	ENSP00000399168.2:n.*390A>G
ENST00000481849.5:n.714A>G
ENST00000497377.5:n.878A>G
NM_005514.6:c.*390A>G	NP_005505.2:n.*390A>G
XM_011514556.1:c.*390A>G	XP_011512858.1:n.*390A>G
XM_011514557.1:c.*390A>G	XP_011512859.1:n.*390A>G
XR_926175.1:n.1918A>G
NM_005514.7:c.*390A>G	NP_005505.2:n.*390A>G
NM_005514.8:c.*390A>G MANE Select	NP_005505.2:n.*390A>G