Canonical Allele Identifier: CA363309209

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355222-C-A
• gnomAD v4: 6-31355222-C-A
• MyVariant Identifiers: chr6:g.31322999C>A (hg19) ; chr6:g.31355222C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355222C>A , CM000668.2:g.31355222C>A	GRCh38
NC_000006.11:g.31322999C>A , CM000668.1:g.31322999C>A	GRCh37
NC_000006.10:g.31430978C>A	NCBI36
NG_023187.1:g.6991G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2944G>T
ENST00000481849.6:n.2463G>T
ENST00000497377.6:n.2370G>T
ENST00000640094.2:c.895+95G>T	ENSP00000491275.2:n.895+95G>T
ENST00000696558.1:c.966G>T	ENSP00000512716.1:n.966G>T
ENST00000696559.1:c.897G>T	ENSP00000512717.1:p.Glu299Asp
ENST00000696560.1:c.897G>T	ENSP00000512718.1:p.Glu299Asp
ENST00000696561.1:c.897G>T	ENSP00000512719.1:p.Glu299Asp
ENST00000696562.1:c.897G>T	ENSP00000512720.1:p.Glu299Asp
ENST00000412585.7:c.897G>T MANE Select	ENSP00000399168.2:p.Glu299Asp
ENST00000640094.1:c.88+95G>T	ENSP00000491275.1:n.88+95G>T
ENST00000412585.6:c.897G>T	ENSP00000399168.2:p.Glu299Asp
ENST00000463574.1:n.488G>T
NM_005514.6:c.897G>T	NP_005505.2:p.Glu299Asp
XM_011514556.1:c.930G>T	XP_011512858.1:p.Glu310Asp
XM_011514557.1:c.895+95G>T	XP_011512859.1:n.895+95G>T
XR_926175.1:n.1336G>T
NM_005514.7:c.897G>T	NP_005505.2:p.Glu299Asp
NM_005514.8:c.897G>T MANE Select	NP_005505.2:p.Glu299Asp