Canonical Allele Identifier: CA1588740029
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585904A= , CM000667.2:g.145585904A= GRCh38
NC_000005.9:g.144965467A= , CM000667.1:g.144965467A= GRCh37
NC_000005.8:g.144945660A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112589T=
XR_944308.1:n.662+179027T=