Canonical Allele Identifier: CA449650052

Gene: HCP5

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463907C>A , CM000668.2:g.31463907C>A	GRCh38
NC_000006.11:g.31431684C>A , CM000668.1:g.31431684C>A	GRCh37
NC_000006.10:g.31539663C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.637C>A