Canonical Allele Identifier: CA136832726
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341362
MyVariant Identifiers: chr6:g.31323131C>T (hg19) chr6:g.31355354C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355354C>T , CM000668.2:g.31355354C>T GRCh38
NC_000006.11:g.31323131C>T , CM000668.1:g.31323131C>T GRCh37
NC_000006.10:g.31431110C>T NCBI36
NG_023187.1:g.6859G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2905G>A
ENST00000481849.6:n.2331G>A
ENST00000497377.6:n.2331G>A
ENST00000640094.2:c.858G>A ENSP00000491275.2:p.Gln286=
ENST00000696558.1:c.927G>A ENSP00000512716.1:n.927G>A
ENST00000696559.1:c.858G>A ENSP00000512717.1:p.Gln286=
ENST00000696560.1:c.858G>A ENSP00000512718.1:p.Gln286=
ENST00000696561.1:c.858G>A ENSP00000512719.1:p.Gln286=
ENST00000696562.1:c.858G>A ENSP00000512720.1:p.Gln286=
ENST00000412585.7:c.858G>A MANE Select ENSP00000399168.2:p.Gln286=
ENST00000640094.1:c.51G>A ENSP00000491275.1:p.Gln17=
ENST00000412585.6:c.858G>A ENSP00000399168.2:p.Gln286=
ENST00000463574.1:n.449G>A
NM_005514.6:c.858G>A NP_005505.2:p.Gln286=
XM_011514556.1:c.891G>A XP_011512858.1:p.Gln297=
XM_011514557.1:c.858G>A XP_011512859.1:p.Gln286=
XR_926175.1:n.1297G>A
NM_005514.7:c.858G>A NP_005505.2:p.Gln286=
NM_005514.8:c.858G>A MANE Select NP_005505.2:p.Gln286=
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