Canonical Allele Identifier: CA136836580
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs151341130

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356816C>G , CM000668.2:g.31356816C>G GRCh38
NC_000006.10:g.31432572C>G NCBI36
NC_000006.11:g.31324593C>G , CM000668.1:g.31324593C>G GRCh37
NG_023187.1:g.5397G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000412585.6:c.215G>C ENSP00000399168.2:p.Arg72Pro
ENST00000434333.1:c.248G>C ENSP00000405931.1:p.Arg83Pro
ENST00000474381.1:n.90G>C
ENST00000498007.1:n.236G>C
ENST00000603274.1:n.170C>G
NM_005514.6:c.215G>C NP_005505.2:p.Arg72Pro
XM_011514556.1:c.248G>C XP_011512858.1:p.Arg83Pro
XM_011514557.1:c.215G>C XP_011512859.1:p.Arg72Pro
XR_926175.1:n.225G>C