Canonical Allele Identifier: CA1588627002
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753411744

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145353924T>A , CM000667.2:g.145353924T>A GRCh38
NC_000005.9:g.144733487T>A , CM000667.1:g.144733487T>A GRCh37
NC_000005.8:g.144713680T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944308.1:n.795-15547A>T