Canonical Allele Identifier: CA923740853

Gene: ZNF886P

Linked Data

• dbSNP Id: rs2045709315

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20004482G>T , CM000686.2:g.20004482G>T	GRCh38
NC_000024.9:g.22166368G>T , CM000686.1:g.22166368G>T	GRCh37
NC_000024.8:g.20625756G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450781.1:n.208+1258C>A