Canonical Allele Identifier: CA2470937977
Gene: ZNF886P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004565A= , CM000686.2:g.20004565A= GRCh38
NC_000024.9:g.22166451A= , CM000686.1:g.22166451A= GRCh37
NC_000024.8:g.20625839A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1175T=