Canonical Allele Identifier: CA136833491

Gene: HLA-B

Linked Data

• dbSNP Id: rs281864637
• gnomAD v4: 6-31356169-G-C
• MyVariant Identifiers: chr6:g.31323946G>C (hg19) ; chr6:g.31356169G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356169G>C , CM000668.2:g.31356169G>C	GRCh38
NC_000006.11:g.31323946G>C , CM000668.1:g.31323946G>C	GRCh37
NC_000006.10:g.31431925G>C	NCBI36
NG_023187.1:g.6044C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2090C>G
ENST00000481849.6:n.2090C>G
ENST00000497377.6:n.2090C>G
ENST00000640094.2:c.617C>G	ENSP00000491275.2:p.Ala206Gly
ENST00000696558.1:c.617C>G	ENSP00000512716.1:p.Ala206Gly
ENST00000696559.1:c.617C>G	ENSP00000512717.1:p.Ala206Gly
ENST00000696560.1:c.617C>G	ENSP00000512718.1:p.Ala206Gly
ENST00000696561.1:c.617C>G	ENSP00000512719.1:p.Ala206Gly
ENST00000696562.1:c.617C>G	ENSP00000512720.1:p.Ala206Gly
ENST00000412585.7:c.617C>G MANE Select	ENSP00000399168.2:p.Ala206Gly
ENST00000412585.6:c.617C>G	ENSP00000399168.2:p.Ala206Gly
ENST00000434333.1:c.650C>G	ENSP00000405931.1:p.Ala217Gly
ENST00000474381.1:n.492C>G
ENST00000498007.1:n.883C>G
NM_005514.6:c.617C>G	NP_005505.2:p.Ala206Gly
XM_011514556.1:c.650C>G	XP_011512858.1:p.Ala217Gly
XM_011514557.1:c.617C>G	XP_011512859.1:p.Ala206Gly
XR_926175.1:n.627C>G
NM_005514.7:c.617C>G	NP_005505.2:p.Ala206Gly
NM_005514.8:c.617C>G MANE Select	NP_005505.2:p.Ala206Gly