Canonical Allele Identifier: CA363308005

Gene: HLA-B

Linked Data

• dbSNP Id: rs1247136475
• gnomAD v4: 6-31354520-T-A
• MyVariant Identifiers: chr6:g.31322297T>A (hg19) ; chr6:g.31354520T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354520T>A , CM000668.2:g.31354520T>A	GRCh38
NC_000006.11:g.31322297T>A , CM000668.1:g.31322297T>A	GRCh37
NC_000006.10:g.31430276T>A	NCBI36
NG_023187.1:g.7693A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3099A>T
ENST00000481849.6:n.3059A>T
ENST00000497377.6:n.2966A>T
ENST00000640094.2:c.935A>T	ENSP00000491275.2:p.Asp312Val
ENST00000696558.1:c.1121A>T	ENSP00000512716.1:n.1121A>T
ENST00000696559.1:c.1052A>T	ENSP00000512717.1:p.Asp351Val
ENST00000696560.1:c.1052A>T	ENSP00000512718.1:p.Asp351Val
ENST00000696561.1:c.1052A>T	ENSP00000512719.1:p.Asp351Val
ENST00000696562.1:c.1052A>T	ENSP00000512720.1:p.Asp351Val
ENST00000412585.7:c.1052A>T MANE Select	ENSP00000399168.2:p.Asp351Val
ENST00000640094.1:c.128A>T	ENSP00000491275.1:p.Asp43Val
ENST00000412585.6:c.1052A>T	ENSP00000399168.2:p.Asp351Val
ENST00000481849.5:n.287A>T
ENST00000497377.5:n.451A>T
NM_005514.6:c.1052A>T	NP_005505.2:p.Asp351Val
XM_011514556.1:c.1085A>T	XP_011512858.1:p.Asp362Val
XM_011514557.1:c.935A>T	XP_011512859.1:p.Asp312Val
XR_926175.1:n.1491A>T
NM_005514.7:c.1052A>T	NP_005505.2:p.Asp351Val
NM_005514.8:c.1052A>T MANE Select	NP_005505.2:p.Asp351Val