Canonical Allele Identifier: CA14809385

Gene: ZNF663P

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46449335G>A , CM000682.2:g.46449335G>A	GRCh38
NC_000020.10:g.45077974G>A , CM000682.1:g.45077974G>A	GRCh37
NC_000020.9:g.44511381G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400371.2:n.1985+6560C>T