Canonical Allele Identifier: CA449650068

Gene: HCP5

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463912T>C , CM000668.2:g.31463912T>C	GRCh38
NC_000006.11:g.31431689T>C , CM000668.1:g.31431689T>C	GRCh37
NC_000006.10:g.31539668T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.642T>C