Canonical Allele Identifier: CA923740970
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs770376273

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