Canonical Allele Identifier: CA2366675049
Gene: ZNF663P HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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