Canonical Allele Identifier: CA3711334

Gene: HLA-B

Linked Data

• dbSNP Id: rs766434800
• ExAC: 6:31323118 G / A
• gnomAD v2: 6-31323118-G-A
• gnomAD v4: 6-31355341-G-A
• MyVariant Identifiers: chr6:g.31323118G>A (hg19) ; chr6:g.31355341G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355341G>A , CM000668.2:g.31355341G>A	GRCh38
NC_000006.11:g.31323118G>A , CM000668.1:g.31323118G>A	GRCh37
NC_000006.10:g.31431097G>A	NCBI36
NG_023187.1:g.6872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2918C>T
ENST00000481849.6:n.2344C>T
ENST00000497377.6:n.2344C>T
ENST00000640094.2:c.871C>T	ENSP00000491275.2:p.Pro291Ser
ENST00000696558.1:c.940C>T	ENSP00000512716.1:n.940C>T
ENST00000696559.1:c.871C>T	ENSP00000512717.1:p.Pro291Ser
ENST00000696560.1:c.871C>T	ENSP00000512718.1:p.Pro291Ser
ENST00000696561.1:c.871C>T	ENSP00000512719.1:p.Pro291Ser
ENST00000696562.1:c.871C>T	ENSP00000512720.1:p.Pro291Ser
ENST00000412585.7:c.871C>T MANE Select	ENSP00000399168.2:p.Pro291Ser
ENST00000640094.1:c.64C>T	ENSP00000491275.1:p.Pro22Ser
ENST00000412585.6:c.871C>T	ENSP00000399168.2:p.Pro291Ser
ENST00000463574.1:n.462C>T
NM_005514.6:c.871C>T	NP_005505.2:p.Pro291Ser
XM_011514556.1:c.904C>T	XP_011512858.1:p.Pro302Ser
XM_011514557.1:c.871C>T	XP_011512859.1:p.Pro291Ser
XR_926175.1:n.1310C>T
NM_005514.7:c.871C>T	NP_005505.2:p.Pro291Ser
NM_005514.8:c.871C>T MANE Select	NP_005505.2:p.Pro291Ser