Canonical Allele Identifier: CA1588740105
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1753151707

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586050C>T , CM000667.2:g.145586050C>T GRCh38
NC_000005.9:g.144965613C>T , CM000667.1:g.144965613C>T GRCh37
NC_000005.8:g.144945806C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112735G>A
XR_944308.1:n.662+178881G>A