Canonical Allele Identifier: CA923741180
Gene: ZNF886P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004669_20004678dup , CM000686.2:g.20004669_20004678dup GRCh38
NC_000024.9:g.22166555_22166564dup , CM000686.1:g.22166555_22166564dup GRCh37
NC_000024.8:g.20625943_20625952dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1081_208+1090dup