Canonical Allele Identifier: CA2366674521
Gene: ZNF663P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46448270A= , CM000682.2:g.46448270A= GRCh38
NC_000020.10:g.45076909A= , CM000682.1:g.45076909A= GRCh37
NC_000020.9:g.44510316A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400371.2:n.1985+7625T=