Canonical Allele Identifier: CA1082551531
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753152748

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586155C>A , CM000667.2:g.145586155C>A GRCh38
NC_000005.9:g.144965718C>A , CM000667.1:g.144965718C>A GRCh37
NC_000005.8:g.144945911C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112840G>T
XR_944308.1:n.662+178776G>T