Canonical Allele Identifier: CA449312463
Gene: HCG4 HGNC NCBI
HLA-V HGNC NCBI

Linked Data

gnomAD v4: 6-29792481-G-T
MyVariant Identifiers: chr6:g.29760258G>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000418983.1:n.270C>A (HCG4)
ENST00000429037.2:n.117G>T (HLA-V)
ENST00000446817.1:n.227G>T (HLA-V)
ENST00000457107.5:n.128G>T (HLA-V)
ENST00000476601.5:n.445G>T (HLA-V)
NM_001207043.1:c.343G>T NP_001193972.1:p.Gly115Cys
NR_002139.2:n.593C>A (HCG4)
NR_132323.1:n.445G>T
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