ClinGen Allele Registry
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Canonical Allele Identifier:
CA2366675049
Gene: ZNF663P
HGNC
NCBI
Linked Data - NCBI & NCI
dbSNP:
460869
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'