Canonical Allele Identifier: CA136832713
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341363
MyVariant Identifiers: chr6:g.31323119C>A (hg19) chr6:g.31355342C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355342C>A , CM000668.2:g.31355342C>A GRCh38
NC_000006.11:g.31323119C>A , CM000668.1:g.31323119C>A GRCh37
NC_000006.10:g.31431098C>A NCBI36
NG_023187.1:g.6871G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2917G>T
ENST00000481849.6:n.2343G>T
ENST00000497377.6:n.2343G>T
ENST00000640094.2:c.870G>T ENSP00000491275.2:p.Leu290=
ENST00000696558.1:c.939G>T ENSP00000512716.1:n.939G>T
ENST00000696559.1:c.870G>T ENSP00000512717.1:p.Leu290=
ENST00000696560.1:c.870G>T ENSP00000512718.1:p.Leu290=
ENST00000696561.1:c.870G>T ENSP00000512719.1:p.Leu290=
ENST00000696562.1:c.870G>T ENSP00000512720.1:p.Leu290=
ENST00000412585.7:c.870G>T MANE Select ENSP00000399168.2:p.Leu290=
ENST00000640094.1:c.63G>T ENSP00000491275.1:p.Leu21=
ENST00000412585.6:c.870G>T ENSP00000399168.2:p.Leu290=
ENST00000463574.1:n.461G>T
NM_005514.6:c.870G>T NP_005505.2:p.Leu290=
XM_011514556.1:c.903G>T XP_011512858.1:p.Leu301=
XM_011514557.1:c.870G>T XP_011512859.1:p.Leu290=
XR_926175.1:n.1309G>T
NM_005514.7:c.870G>T NP_005505.2:p.Leu290=
NM_005514.8:c.870G>T MANE Select NP_005505.2:p.Leu290=
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