Canonical Allele Identifier: CA449312497

Linked Data

MyVariant Identifiers: chr6:g.29760266G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29792489G>C , CM000668.2:g.29792489G>C GRCh38
NC_000006.11:g.29760266G>C , CM000668.1:g.29760266G>C GRCh37
NC_000006.10:g.29868245G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.262C>G (HCG4)
ENST00000429037.2:n.125G>C (HLA-V)
ENST00000446817.1:n.235G>C (HLA-V)
ENST00000457107.5:n.136G>C (HLA-V)
ENST00000476601.5:n.453G>C (HLA-V)
NM_001207043.1:c.351G>C NP_001193972.1:p.Ala117=
NR_002139.2:n.585C>G (HCG4)
NR_132323.1:n.453G>C