Canonical Allele Identifier: CA2240994106
Gene: ZNF469 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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