Canonical Allele Identifier: CA449601237

Gene: HLA-B

Linked Data

• dbSNP Id: rs1582541701
• gnomAD v3: 6-31355129-C-A
• gnomAD v4: 6-31355129-C-A
• MyVariant Identifiers: chr6:g.31322906C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355129C>A , CM000668.2:g.31355129C>A	GRCh38
NC_000006.11:g.31322906C>A , CM000668.1:g.31322906C>A	GRCh37
NC_000006.10:g.31430885C>A	NCBI36
NG_023187.1:g.7084G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3037G>T
ENST00000481849.6:n.2556G>T
ENST00000497377.6:n.2463G>T
ENST00000640094.2:c.895+188G>T	ENSP00000491275.2:n.895+188G>T
ENST00000696558.1:c.1059G>T	ENSP00000512716.1:n.1059G>T
ENST00000696559.1:c.990G>T	ENSP00000512717.1:p.Val330=
ENST00000696560.1:c.990G>T	ENSP00000512718.1:p.Val330=
ENST00000696561.1:c.990G>T	ENSP00000512719.1:p.Val330=
ENST00000696562.1:c.990G>T	ENSP00000512720.1:p.Val330=
ENST00000412585.7:c.990G>T MANE Select	ENSP00000399168.2:p.Val330=
ENST00000640094.1:c.88+188G>T	ENSP00000491275.1:n.88+188G>T
ENST00000412585.6:c.990G>T	ENSP00000399168.2:p.Val330=
ENST00000463574.1:n.581G>T
NM_005514.6:c.990G>T	NP_005505.2:p.Val330=
XM_011514556.1:c.1023G>T	XP_011512858.1:p.Val341=
XM_011514557.1:c.895+188G>T	XP_011512859.1:n.895+188G>T
XR_926175.1:n.1429G>T
NM_005514.7:c.990G>T	NP_005505.2:p.Val330=
NM_005514.8:c.990G>T MANE Select	NP_005505.2:p.Val330=