Canonical Allele Identifier: CA14814305
Gene: ZNF663P HGNC NCBI

Linked Data

dbSNP Id: rs460703

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46453203G>A , CM000682.2:g.46453203G>A GRCh38
NC_000020.10:g.45081842G>A , CM000682.1:g.45081842G>A GRCh37
NC_000020.9:g.44515249G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000400371.2:n.1985+2692C>T