Canonical Allele Identifier: CA449650070

Gene: HCP5

Linked Data - Variant Effect Evidence

Genomic Alleles

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

Transcript Alleles

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