Canonical Allele Identifier: CA135991568

Linked Data

dbSNP Id: rs907565065

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792486C>G , CM000668.2:g.29792486C>G GRCh38
NC_000006.11:g.29760263C>G , CM000668.1:g.29760263C>G GRCh37
NC_000006.10:g.29868242C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.265G>C (HCG4)
ENST00000429037.2:n.122C>G (HLA-V)
ENST00000446817.1:n.232C>G (HLA-V)
ENST00000457107.5:n.133C>G (HLA-V)
ENST00000476601.5:n.450C>G (HLA-V)
NM_001207043.1:c.348C>G NP_001193972.1:p.Arg116=
NR_002139.2:n.588G>C (HCG4)
NR_132323.1:n.450C>G