Canonical Allele Identifier: CA3711990
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050462

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357134C>G , CM000668.2:g.31357134C>G GRCh38
NC_000006.11:g.31324911C>G , CM000668.1:g.31324911C>G GRCh37
NC_000006.10:g.31432890C>G NCBI36
NG_023187.1:g.5079G>C

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.25G>C VV NP_005505.2:p.Val9Leu
XM_011514557.1:c.25G>C XP_011512859.1:p.Val9Leu
XR_926175.1:n.35G>C
NM_005514.7:c.25G>C VV NP_005505.2:p.Val9Leu
NM_005514.8:c.25G>C VV MANE Preferred NP_005505.2:p.Val9Leu
ENST00000412585.6:c.25G>C ENSP00000399168.2:p.Val9Leu
ENST00000434333.1:c.-71G>C ENSP00000405931.1:p.=
ENST00000498007.1:n.46G>C
ENST00000603274.1:n.488C>G