Canonical Allele Identifier: CA1588740149
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753152862

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586162G>A , CM000667.2:g.145586162G>A GRCh38
NC_000005.9:g.144965725G>A , CM000667.1:g.144965725G>A GRCh37
NC_000005.8:g.144945918G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112847C>T
XR_944308.1:n.662+178769C>T