Canonical Allele Identifier: CA363307891

Gene: HLA-B

Linked Data

• dbSNP Id: rs1377561203
• gnomAD v4: 6-31354499-A-G
• MyVariant Identifiers: chr6:g.31322276A>G (hg19) ; chr6:g.31354499A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354499A>G , CM000668.2:g.31354499A>G	GRCh38
NC_000006.11:g.31322276A>G , CM000668.1:g.31322276A>G	GRCh37
NC_000006.10:g.31430255A>G	NCBI36
NG_023187.1:g.7714T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3120T>C
ENST00000481849.6:n.3080T>C
ENST00000497377.6:n.2987T>C
ENST00000640094.2:c.956T>C	ENSP00000491275.2:p.Val319Ala
ENST00000696558.1:c.1142T>C	ENSP00000512716.1:n.1142T>C
ENST00000696559.1:c.1073T>C	ENSP00000512717.1:p.Val358Ala
ENST00000696560.1:c.1073T>C	ENSP00000512718.1:p.Val358Ala
ENST00000696561.1:c.1073T>C	ENSP00000512719.1:p.Val358Ala
ENST00000696562.1:c.1073T>C	ENSP00000512720.1:p.Val358Ala
ENST00000412585.7:c.1073T>C MANE Select	ENSP00000399168.2:p.Val358Ala
ENST00000412585.6:c.1073T>C	ENSP00000399168.2:p.Val358Ala
ENST00000481849.5:n.308T>C
ENST00000497377.5:n.472T>C
NM_005514.6:c.1073T>C	NP_005505.2:p.Val358Ala
XM_011514556.1:c.1106T>C	XP_011512858.1:p.Val369Ala
XM_011514557.1:c.956T>C	XP_011512859.1:p.Val319Ala
XR_926175.1:n.1512T>C
NM_005514.7:c.1073T>C	NP_005505.2:p.Val358Ala
NM_005514.8:c.1073T>C MANE Select	NP_005505.2:p.Val358Ala