Canonical Allele Identifier: CA449652129

Gene: HCP5

Linked Data

• dbSNP Id: rs1762878743
• gnomAD v4: 6-31464384-C-A
• MyVariant Identifiers: chr6:g.31432161C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464384C>A , CM000668.2:g.31464384C>A	GRCh38
NC_000006.11:g.31432161C>A , CM000668.1:g.31432161C>A	GRCh37
NC_000006.10:g.31540140C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.1114C>A