Canonical Allele Identifier: CA136836645
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs151341107

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356881G>A , CM000668.2:g.31356881G>A GRCh38
NC_000006.11:g.31324658G>A , CM000668.1:g.31324658G>A GRCh37
NC_000006.10:g.31432637G>A NCBI36
NG_023187.1:g.5332C>T

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.150C>T VV NP_005505.2:p.Gly50=
XM_011514556.1:c.183C>T XP_011512858.1:p.Gly61=
XM_011514557.1:c.150C>T XP_011512859.1:p.Gly50=
XR_926175.1:n.160C>T
NM_005514.7:c.150C>T VV NP_005505.2:p.Gly50=
NM_005514.8:c.150C>T VV MANE Preferred NP_005505.2:p.Gly50=
ENST00000412585.6:c.150C>T ENSP00000399168.2:p.Gly50=
ENST00000434333.1:c.183C>T ENSP00000405931.1:p.Gly61=
ENST00000474381.1:n.25C>T
ENST00000498007.1:n.171C>T
ENST00000603274.1:n.235G>A