Canonical Allele Identifier: CA363310330
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355374T>C , CM000668.2:g.31355374T>C GRCh38
NC_000006.11:g.31323151T>C , CM000668.1:g.31323151T>C GRCh37
NC_000006.10:g.31431130T>C NCBI36
NG_023187.1:g.6839A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2885A>G
ENST00000481849.6:n.2311A>G
ENST00000497377.6:n.2311A>G
ENST00000640094.2:c.838A>G ENSP00000491275.2:p.Arg280Gly
ENST00000696558.1:c.907A>G ENSP00000512716.1:n.907A>G
ENST00000696559.1:c.838A>G ENSP00000512717.1:p.Arg280Gly
ENST00000696560.1:c.838A>G ENSP00000512718.1:p.Arg280Gly
ENST00000696561.1:c.838A>G ENSP00000512719.1:p.Arg280Gly
ENST00000696562.1:c.838A>G ENSP00000512720.1:p.Arg280Gly
ENST00000412585.7:c.838A>G MANE Select ENSP00000399168.2:p.Arg280Gly
ENST00000640094.1:c.31A>G ENSP00000491275.1:p.Arg11Gly
ENST00000412585.6:c.838A>G ENSP00000399168.2:p.Arg280Gly
ENST00000463574.1:n.429A>G
NM_005514.6:c.838A>G NP_005505.2:p.Arg280Gly
XM_011514556.1:c.871A>G XP_011512858.1:p.Arg291Gly
XM_011514557.1:c.838A>G XP_011512859.1:p.Arg280Gly
XR_926175.1:n.1277A>G
NM_005514.7:c.838A>G NP_005505.2:p.Arg280Gly
NM_005514.8:c.838A>G MANE Select NP_005505.2:p.Arg280Gly