Canonical Allele Identifier: CA449312453

Linked Data

MyVariant Identifiers: chr6:g.29760256C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000418983.1:n.272G>A (HCG4)
ENST00000429037.2:n.115C>T (HLA-V)
ENST00000446817.1:n.225C>T (HLA-V)
ENST00000457107.5:n.126C>T (HLA-V)
ENST00000476601.5:n.443C>T (HLA-V)
NM_001207043.1:c.341C>T NP_001193972.1:p.Pro114Leu
NR_002139.2:n.595G>A (HCG4)
NR_132323.1:n.443C>T