Canonical Allele Identifier: CA923740865
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs2045709334

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004541T>G , CM000686.2:g.20004541T>G GRCh38
NC_000024.9:g.22166427T>G , CM000686.1:g.22166427T>G GRCh37
NC_000024.8:g.20625815T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1199A>C