Canonical Allele Identifier: CA449650221

Gene: HCP5

Linked Data

• dbSNP Id: rs1762859491
• gnomAD v3: 6-31463967-C-G
• gnomAD v4: 6-31463967-C-G
• MyVariant Identifiers: chr6:g.31431744C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463967C>G , CM000668.2:g.31463967C>G	GRCh38
NC_000006.11:g.31431744C>G , CM000668.1:g.31431744C>G	GRCh37
NC_000006.10:g.31539723C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.697C>G