Canonical Allele Identifier: CA449790725

Gene: HLA-B

Linked Data

• dbSNP Id: rs937187651
• gnomAD v3: 6-31355570-G-A
• gnomAD v4: 6-31355570-G-A
• MyVariant Identifiers: chr6:g.31323347G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355570G>A , CM000668.2:g.31355570G>A	GRCh38
NC_000006.11:g.31323347G>A , CM000668.1:g.31323347G>A	GRCh37
NC_000006.10:g.31431326G>A	NCBI36
NG_023187.1:g.6643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2689C>T
ENST00000481849.6:n.2115C>T
ENST00000497377.6:n.2115C>T
ENST00000640094.2:c.642C>T	ENSP00000491275.2:p.Thr214=
ENST00000696558.1:c.711C>T	ENSP00000512716.1:n.711C>T
ENST00000696559.1:c.642C>T	ENSP00000512717.1:p.Thr214=
ENST00000696560.1:c.642C>T	ENSP00000512718.1:p.Thr214=
ENST00000696561.1:c.642C>T	ENSP00000512719.1:p.Thr214=
ENST00000696562.1:c.642C>T	ENSP00000512720.1:p.Thr214=
ENST00000412585.7:c.642C>T MANE Select	ENSP00000399168.2:p.Thr214=
ENST00000412585.6:c.642C>T	ENSP00000399168.2:p.Thr214=
ENST00000434333.1:c.675C>T	ENSP00000405931.1:p.Thr225=
ENST00000463574.1:n.233C>T
ENST00000474381.1:n.1091C>T
ENST00000498007.1:n.908C>T
NM_005514.6:c.642C>T	NP_005505.2:p.Thr214=
XM_011514556.1:c.675C>T	XP_011512858.1:p.Thr225=
XM_011514557.1:c.642C>T	XP_011512859.1:p.Thr214=
XR_926175.1:n.1081C>T
NM_005514.7:c.642C>T	NP_005505.2:p.Thr214=
NM_005514.8:c.642C>T MANE Select	NP_005505.2:p.Thr214=