Canonical Allele Identifier: CA136835939
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs151341237

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356379C>T , CM000668.2:g.31356379C>T GRCh38
NC_000006.10:g.31432135C>T NCBI36
NC_000006.11:g.31324156C>T , CM000668.1:g.31324156C>T GRCh37
NG_023187.1:g.5834G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000412585.6:c.407G>A ENSP00000399168.2:p.Gly136Glu
ENST00000434333.1:c.440G>A ENSP00000405931.1:p.Gly147Glu
ENST00000474381.1:n.282G>A
ENST00000498007.1:n.673G>A
NM_005514.6:c.407G>A VV NP_005505.2:p.Gly136Glu
XM_011514556.1:c.440G>A XP_011512858.1:p.Gly147Glu
XM_011514557.1:c.407G>A XP_011512859.1:p.Gly136Glu
XR_926175.1:n.417G>A