Canonical Allele Identifier: CA2470937974
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs1603548765

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004525A>G , CM000686.2:g.20004525A>G GRCh38
NC_000024.9:g.22166411A>G , CM000686.1:g.22166411A>G GRCh37
NC_000024.8:g.20625799A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000450781.1:n.208+1215T>C