ClinGen Allele Registry
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Canonical Allele Identifier:
CA923740970
Gene: ZNF886P
HGNC
NCBI
Linked Data
dbSNP Id:
rs770376273
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20004678del , CM000686.2:g.20004678del
GRCh38
NC_000024.9:g.22166564del , CM000686.1:g.22166564del
GRCh37
NC_000024.8:g.20625952del
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000450781.1:n.208+1090del
Search 100 bp 5'
Search 100 bp 3'