Canonical Allele Identifier: CA449313102

Gene: HCG4 HLA-V

Linked Data

• gnomAD v4: 6-29792583-C-T
• MyVariant Identifiers: chr6:g.29760360C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29792583C>T , CM000668.2:g.29792583C>T	GRCh38
NC_000006.11:g.29760360C>T , CM000668.1:g.29760360C>T	GRCh37
NC_000006.10:g.29868339C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000418983.1:n.168G>A (HCG4)
ENST00000429037.2:n.219C>T (HLA-V)
ENST00000446817.1:n.329C>T (HLA-V)
ENST00000457107.5:n.230C>T (HLA-V)
ENST00000476601.5:n.547C>T (HLA-V)
NM_001207043.1:c.445C>T	NP_001193972.1:p.Pro149Ser
NR_002139.2:n.491G>A (HCG4)
NR_132323.1:n.547C>T