Canonical Allele Identifier: CA3711883
Gene: HLA-B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050486

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356925C>T , CM000668.2:g.31356925C>T GRCh38
NC_000006.11:g.31324702C>T , CM000668.1:g.31324702C>T GRCh37
NC_000006.10:g.31432681C>T NCBI36
NG_023187.1:g.5288G>A

Transcript Alleles

HGVS Amino-acid change
NM_005514.6:c.106G>A VV NP_005505.2:p.Val36Met
XM_011514556.1:c.139G>A XP_011512858.1:p.Val47Met
XM_011514557.1:c.106G>A XP_011512859.1:p.Val36Met
XR_926175.1:n.116G>A
NM_005514.7:c.106G>A VV NP_005505.2:p.Val36Met
NM_005514.8:c.106G>A VV MANE Preferred NP_005505.2:p.Val36Met
ENST00000412585.6:c.106G>A ENSP00000399168.2:p.Val36Met
ENST00000434333.1:c.139G>A ENSP00000405931.1:p.Val47Met
ENST00000498007.1:n.127G>A
ENST00000603274.1:n.279C>T