Canonical Allele Identifier: CA136836744

Gene: HLA-B

Linked Data

• dbSNP Id: rs151341076
• gnomAD v4: 6-31357087-G-C
• MyVariant Identifiers: chr6:g.31324864G>C (hg19) ; chr6:g.31357087G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357087G>C , CM000668.2:g.31357087G>C	GRCh38
NC_000006.11:g.31324864G>C , CM000668.1:g.31324864G>C	GRCh37
NC_000006.10:g.31432843G>C	NCBI36
NG_023187.1:g.5126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1545C>G
ENST00000481849.6:n.1545C>G
ENST00000497377.6:n.1545C>G
ENST00000640094.2:c.72C>G	ENSP00000491275.2:p.Ala24=
ENST00000696558.1:c.72C>G	ENSP00000512716.1:p.Ala24=
ENST00000696559.1:c.72C>G	ENSP00000512717.1:p.Ala24=
ENST00000696560.1:c.72C>G	ENSP00000512718.1:p.Ala24=
ENST00000696561.1:c.72C>G	ENSP00000512719.1:p.Ala24=
ENST00000696562.1:c.72C>G	ENSP00000512720.1:p.Ala24=
ENST00000412585.7:c.72C>G MANE Select	ENSP00000399168.2:p.Ala24=
ENST00000412585.6:c.72C>G	ENSP00000399168.2:p.Ala24=
ENST00000434333.1:c.-24C>G	ENSP00000405931.1:n.-24C>G
ENST00000498007.1:n.93C>G
ENST00000603274.1:n.441G>C
NM_005514.6:c.72C>G	NP_005505.2:p.Ala24=
XM_011514557.1:c.72C>G	XP_011512859.1:p.Ala24=
XR_926175.1:n.82C>G
NM_005514.7:c.72C>G	NP_005505.2:p.Ala24=
NM_005514.8:c.72C>G MANE Select	NP_005505.2:p.Ala24=