Canonical Allele Identifier: CA449649837

Gene: HCP5

Linked Data

• dbSNP Id: rs1762849403
• gnomAD v4: 6-31463829-A-G
• MyVariant Identifiers: chr6:g.31431606A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463829A>G , CM000668.2:g.31463829A>G	GRCh38
NC_000006.11:g.31431606A>G , CM000668.1:g.31431606A>G	GRCh37
NC_000006.10:g.31539585A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.559A>G