Canonical Allele Identifier: CA449650042

Gene: HCP5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463903G>T , CM000668.2:g.31463903G>T	GRCh38
NC_000006.11:g.31431680G>T , CM000668.1:g.31431680G>T	GRCh37
NC_000006.10:g.31539659G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040662.1:n.633G>T