Canonical Allele Identifier: CA1618450386

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792487G= , CM000668.2:g.29792487G= GRCh38
NC_000006.11:g.29760264G= , CM000668.1:g.29760264G= GRCh37
NC_000006.10:g.29868243G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.264C= (HCG4)
ENST00000429037.2:n.123G= (HLA-V)
ENST00000446817.1:n.233G= (HLA-V)
ENST00000457107.5:n.134G= (HLA-V)
ENST00000476601.5:n.451G= (HLA-V)
NM_001207043.1:c.349G= NP_001193972.1:p.Ala117=
NR_002139.2:n.587C= (HCG4)
NR_132323.1:n.451G=