Canonical Allele Identifier: CA923740966
Gene: ZNF886P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.2:g.20004678_20004679insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000024.9:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000686.1:g.22166564_22166565insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000024.8:g.20625952_20625953insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

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