Canonical Allele Identifier: CA1588739963
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585763C= , CM000667.2:g.145585763C= GRCh38
NC_000005.9:g.144965326C= , CM000667.1:g.144965326C= GRCh37
NC_000005.8:g.144945519C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112448G=
XR_944308.1:n.662+179168G=