Canonical Allele Identifier: CA449648855

Gene: HCP5

Linked Data

• dbSNP Id: rs1762840091
• gnomAD v3: 6-31463641-G-A
• gnomAD v4: 6-31463641-G-A
• MyVariant Identifiers: chr6:g.31431418G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463641G>A , CM000668.2:g.31463641G>A	GRCh38
NC_000006.11:g.31431418G>A , CM000668.1:g.31431418G>A	GRCh37
NC_000006.10:g.31539397G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.371G>A