Canonical Allele Identifier: CA1588740007
Gene: PRELID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145585847C= , CM000667.2:g.145585847C= GRCh38
NC_000005.9:g.144965410C= , CM000667.1:g.144965410C= GRCh37
NC_000005.8:g.144945603C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510259.5:n.71-112532G=
XR_944308.1:n.662+179084G=