Canonical Allele Identifier: CA2366676675
Gene: ZNF663P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46453332A>T , CM000682.2:g.46453332A>T GRCh38
NC_000020.10:g.45081971A>T , CM000682.1:g.45081971A>T GRCh37
NC_000020.9:g.44515378A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400371.2:n.1985+2563T>A