Canonical Allele Identifier: CA449790730

Gene: HLA-B

Linked Data

• dbSNP Id: rs1313356998
• gnomAD v4: 6-31355579-T-C
• MyVariant Identifiers: chr6:g.31323356T>C (hg19) ; chr6:g.31355579T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355579T>C , CM000668.2:g.31355579T>C	GRCh38
NC_000006.11:g.31323356T>C , CM000668.1:g.31323356T>C	GRCh37
NC_000006.10:g.31431335T>C	NCBI36
NG_023187.1:g.6634A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2680A>G
ENST00000481849.6:n.2106A>G
ENST00000497377.6:n.2106A>G
ENST00000640094.2:c.633A>G	ENSP00000491275.2:p.Thr211=
ENST00000696558.1:c.702A>G	ENSP00000512716.1:n.702A>G
ENST00000696559.1:c.633A>G	ENSP00000512717.1:p.Thr211=
ENST00000696560.1:c.633A>G	ENSP00000512718.1:p.Thr211=
ENST00000696561.1:c.633A>G	ENSP00000512719.1:p.Thr211=
ENST00000696562.1:c.633A>G	ENSP00000512720.1:p.Thr211=
ENST00000412585.7:c.633A>G MANE Select	ENSP00000399168.2:p.Thr211=
ENST00000412585.6:c.633A>G	ENSP00000399168.2:p.Thr211=
ENST00000434333.1:c.666A>G	ENSP00000405931.1:p.Thr222=
ENST00000463574.1:n.224A>G
ENST00000474381.1:n.1082A>G
ENST00000498007.1:n.899A>G
NM_005514.6:c.633A>G	NP_005505.2:p.Thr211=
XM_011514556.1:c.666A>G	XP_011512858.1:p.Thr222=
XM_011514557.1:c.633A>G	XP_011512859.1:p.Thr211=
XR_926175.1:n.1072A>G
NM_005514.7:c.633A>G	NP_005505.2:p.Thr211=
NM_005514.8:c.633A>G MANE Select	NP_005505.2:p.Thr211=