Canonical Allele Identifier: CA1618450383

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792481G= , CM000668.2:g.29792481G= GRCh38
NC_000006.11:g.29760258G= , CM000668.1:g.29760258G= GRCh37
NC_000006.10:g.29868237G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.270C= (HCG4)
ENST00000429037.2:n.117G= (HLA-V)
ENST00000446817.1:n.227G= (HLA-V)
ENST00000457107.5:n.128G= (HLA-V)
ENST00000476601.5:n.445G= (HLA-V)
NM_001207043.1:c.343G= NP_001193972.1:p.Gly115=
NR_002139.2:n.593C= (HCG4)
NR_132323.1:n.445G=