Canonical Allele Identifier: CA136836048
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341221
gnomAD v4: 6-31356414-G-C
MyVariant Identifiers: chr6:g.31324191G>C (hg19) chr6:g.31356414G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356414G>C , CM000668.2:g.31356414G>C GRCh38
NC_000006.11:g.31324191G>C , CM000668.1:g.31324191G>C GRCh37
NC_000006.10:g.31432170G>C NCBI36
NG_023187.1:g.5799C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1845C>G
ENST00000481849.6:n.1845C>G
ENST00000497377.6:n.1845C>G
ENST00000640094.2:c.372C>G ENSP00000491275.2:p.Gly124=
ENST00000696558.1:c.372C>G ENSP00000512716.1:p.Gly124=
ENST00000696559.1:c.372C>G ENSP00000512717.1:p.Gly124=
ENST00000696560.1:c.372C>G ENSP00000512718.1:p.Gly124=
ENST00000696561.1:c.372C>G ENSP00000512719.1:p.Gly124=
ENST00000696562.1:c.372C>G ENSP00000512720.1:p.Gly124=
ENST00000412585.7:c.372C>G MANE Select ENSP00000399168.2:p.Gly124=
ENST00000412585.6:c.372C>G ENSP00000399168.2:p.Gly124=
ENST00000434333.1:c.405C>G ENSP00000405931.1:p.Gly135=
ENST00000474381.1:n.247C>G
ENST00000498007.1:n.638C>G
NM_005514.6:c.372C>G NP_005505.2:p.Gly124=
XM_011514556.1:c.405C>G XP_011512858.1:p.Gly135=
XM_011514557.1:c.372C>G XP_011512859.1:p.Gly124=
XR_926175.1:n.382C>G
NM_005514.7:c.372C>G NP_005505.2:p.Gly124=
NM_005514.8:c.372C>G MANE Select NP_005505.2:p.Gly124=
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