Canonical Allele Identifier: CA1082551482
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753150896

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586002G>A , CM000667.2:g.145586002G>A GRCh38
NC_000005.9:g.144965565G>A , CM000667.1:g.144965565G>A GRCh37
NC_000005.8:g.144945758G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112687C>T
XR_944308.1:n.662+178929C>T