Canonical Allele Identifier: CA136834537
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs151341240

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356363G>C , CM000668.2:g.31356363G>C GRCh38
NC_000006.11:g.31324140G>C , CM000668.1:g.31324140G>C GRCh37
NC_000006.10:g.31432119G>C NCBI36
NG_023187.1:g.5850C>G

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.423C>G VV NP_005505.2:p.Ala141=
XM_011514556.1:c.456C>G XP_011512858.1:p.Ala152=
XM_011514557.1:c.423C>G XP_011512859.1:p.Ala141=
XR_926175.1:n.433C>G
NM_005514.7:c.423C>G VV NP_005505.2:p.Ala141=
NM_005514.8:c.423C>G VV MANE Preferred NP_005505.2:p.Ala141=
ENST00000412585.6:c.423C>G ENSP00000399168.2:p.Ala141=
ENST00000434333.1:c.456C>G ENSP00000405931.1:p.Ala152=
ENST00000474381.1:n.298C>G
ENST00000498007.1:n.689C>G