Canonical Allele Identifier: CA1588740141
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586150A= , CM000667.2:g.145586150A= GRCh38
NC_000005.9:g.144965713A= , CM000667.1:g.144965713A= GRCh37
NC_000005.8:g.144945906A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112835T=
XR_944308.1:n.662+178781T=