Canonical Allele Identifier: CA449790728

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766870412
• gnomAD v3: 6-31355573-C-T
• gnomAD v4: 6-31355573-C-T
• MyVariant Identifiers: chr6:g.31323350C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355573C>T , CM000668.2:g.31355573C>T	GRCh38
NC_000006.11:g.31323350C>T , CM000668.1:g.31323350C>T	GRCh37
NC_000006.10:g.31431329C>T	NCBI36
NG_023187.1:g.6640G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2686G>A
ENST00000481849.6:n.2112G>A
ENST00000497377.6:n.2112G>A
ENST00000640094.2:c.639G>A	ENSP00000491275.2:p.Val213=
ENST00000696558.1:c.708G>A	ENSP00000512716.1:n.708G>A
ENST00000696559.1:c.639G>A	ENSP00000512717.1:p.Val213=
ENST00000696560.1:c.639G>A	ENSP00000512718.1:p.Val213=
ENST00000696561.1:c.639G>A	ENSP00000512719.1:p.Val213=
ENST00000696562.1:c.639G>A	ENSP00000512720.1:p.Val213=
ENST00000412585.7:c.639G>A MANE Select	ENSP00000399168.2:p.Val213=
ENST00000412585.6:c.639G>A	ENSP00000399168.2:p.Val213=
ENST00000434333.1:c.672G>A	ENSP00000405931.1:p.Val224=
ENST00000463574.1:n.230G>A
ENST00000474381.1:n.1088G>A
ENST00000498007.1:n.905G>A
NM_005514.6:c.639G>A	NP_005505.2:p.Val213=
XM_011514556.1:c.672G>A	XP_011512858.1:p.Val224=
XM_011514557.1:c.639G>A	XP_011512859.1:p.Val213=
XR_926175.1:n.1078G>A
NM_005514.7:c.639G>A	NP_005505.2:p.Val213=
NM_005514.8:c.639G>A MANE Select	NP_005505.2:p.Val213=