Canonical Allele Identifier: CA3711331

Gene: HLA-B

Linked Data

• dbSNP Id: rs1611623
• ExAC: 6:31323117 G / T
• gnomAD v2: 6-31323117-G-T
• gnomAD v3: 6-31355340-G-T
• gnomAD v4: 6-31355340-G-T
• COSMIC: COSM4160789
• MyVariant Identifiers: chr6:g.31323117G>T (hg19) ; chr6:g.31355340G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355340G>T , CM000668.2:g.31355340G>T	GRCh38
NC_000006.11:g.31323117G>T , CM000668.1:g.31323117G>T	GRCh37
NC_000006.10:g.31431096G>T	NCBI36
NG_023187.1:g.6873C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2919C>A
ENST00000481849.6:n.2345C>A
ENST00000497377.6:n.2345C>A
ENST00000640094.2:c.872C>A	ENSP00000491275.2:p.Pro291Gln
ENST00000696558.1:c.941C>A	ENSP00000512716.1:n.941C>A
ENST00000696559.1:c.872C>A	ENSP00000512717.1:p.Pro291Gln
ENST00000696560.1:c.872C>A	ENSP00000512718.1:p.Pro291Gln
ENST00000696561.1:c.872C>A	ENSP00000512719.1:p.Pro291Gln
ENST00000696562.1:c.872C>A	ENSP00000512720.1:p.Pro291Gln
ENST00000412585.7:c.872C>A MANE Select	ENSP00000399168.2:p.Pro291Gln
ENST00000640094.1:c.65C>A	ENSP00000491275.1:p.Pro22Gln
ENST00000412585.6:c.872C>A	ENSP00000399168.2:p.Pro291Gln
ENST00000463574.1:n.463C>A
NM_005514.6:c.872C>A	NP_005505.2:p.Pro291Gln
XM_011514556.1:c.905C>A	XP_011512858.1:p.Pro302Gln
XM_011514557.1:c.872C>A	XP_011512859.1:p.Pro291Gln
XR_926175.1:n.1311C>A
NM_005514.7:c.872C>A	NP_005505.2:p.Pro291Gln
NM_005514.8:c.872C>A MANE Select	NP_005505.2:p.Pro291Gln