Canonical Allele Identifier: CA923740872
Gene: ZNF886P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004546A>G , CM000686.2:g.20004546A>G GRCh38
NC_000024.9:g.22166432A>G , CM000686.1:g.22166432A>G GRCh37
NC_000024.8:g.20625820A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1194T>C