Canonical Allele Identifier: CA1618450380

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792479C= , CM000668.2:g.29792479C= GRCh38
NC_000006.11:g.29760256C= , CM000668.1:g.29760256C= GRCh37
NC_000006.10:g.29868235C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.272G= (HCG4)
ENST00000429037.2:n.115C= (HLA-V)
ENST00000446817.1:n.225C= (HLA-V)
ENST00000457107.5:n.126C= (HLA-V)
ENST00000476601.5:n.443C= (HLA-V)
NM_001207043.1:c.341C= NP_001193972.1:p.Pro114=
NR_002139.2:n.595G= (HCG4)
NR_132323.1:n.443C=