Canonical Allele Identifier: CA14234489

Gene: ZNF469

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88298034C>A , CM000678.2:g.88298034C>A	GRCh38
NC_000016.9:g.88331640C>A , CM000678.1:g.88331640C>A	GRCh37
NC_000016.8:g.86889141C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011523386.1:c.-192+21459C>A	XP_011521688.1:n.-192+21459C>A