Canonical Allele Identifier: CA923740881
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs2045709365
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004598G>A , CM000686.2:g.20004598G>A GRCh38
NC_000024.9:g.22166484G>A , CM000686.1:g.22166484G>A GRCh37
NC_000024.8:g.20625872G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450781.1:n.208+1142C>T
Search 100 bp 5'
Search 100 bp 3'