Canonical Allele Identifier: CA449650061

Gene: HCP5

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463910C>G , CM000668.2:g.31463910C>G	GRCh38
NC_000006.11:g.31431687C>G , CM000668.1:g.31431687C>G	GRCh37
NC_000006.10:g.31539666C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.640C>G