Canonical Allele Identifier: CA3691577

Gene: HCG4 HLA-V

Linked Data

• dbSNP Id: rs11539957
• ExAC: 6:29760354 C / A
• gnomAD v2: 6-29760354-C-A
• gnomAD v4: 6-29792577-C-A
• MyVariant Identifiers: chr6:g.29760354C>A (hg19) ; chr6:g.29792577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29792577C>A , CM000668.2:g.29792577C>A	GRCh38
NC_000006.11:g.29760354C>A , CM000668.1:g.29760354C>A	GRCh37
NC_000006.10:g.29868333C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000418983.1:n.174G>T (HCG4)
ENST00000429037.2:n.213C>A (HLA-V)
ENST00000446817.1:n.323C>A (HLA-V)
ENST00000457107.5:n.224C>A (HLA-V)
ENST00000476601.5:n.541C>A (HLA-V)
NM_001207043.1:c.439C>A	NP_001193972.1:p.Arg147=
NR_002139.2:n.497G>T (HCG4)
NR_132323.1:n.541C>A