Canonical Allele Identifier: CA449650047

Gene: HCP5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463905C>T , CM000668.2:g.31463905C>T	GRCh38
NC_000006.11:g.31431682C>T , CM000668.1:g.31431682C>T	GRCh37
NC_000006.10:g.31539661C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.635C>T