Canonical Allele Identifier: CA449650357

Gene: HCP5

Linked Data

• gnomAD v4: 6-31464016-G-A
• MyVariant Identifiers: chr6:g.31431793G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31464016G>A , CM000668.2:g.31464016G>A	GRCh38
NC_000006.11:g.31431793G>A , CM000668.1:g.31431793G>A	GRCh37
NC_000006.10:g.31539772G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.746G>A