Canonical Allele Identifier: CA1588739972
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585787T= , CM000667.2:g.145585787T= GRCh38
NC_000005.9:g.144965350T= , CM000667.1:g.144965350T= GRCh37
NC_000005.8:g.144945543T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112472A=
XR_944308.1:n.662+179144A=