Canonical Allele Identifier: CA923741251
Gene: ZNF886P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004665_20004678dup , CM000686.2:g.20004665_20004678dup GRCh38
NC_000024.9:g.22166551_22166564dup , CM000686.1:g.22166551_22166564dup GRCh37
NC_000024.8:g.20625939_20625952dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1077_208+1090dup