Canonical Allele Identifier: CA923741214
Gene: ZNF886P HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.2:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000024.9:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.1:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000024.8:g.20625952_20625953insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1090_208+1091insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Search 100 bp 5'
Search 100 bp 3'