Canonical Allele Identifier: CA449650071

Gene: HCP5

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463913G>T , CM000668.2:g.31463913G>T	GRCh38
NC_000006.11:g.31431690G>T , CM000668.1:g.31431690G>T	GRCh37
NC_000006.10:g.31539669G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.643G>T