Canonical Allele Identifier: CA129525443
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs896778976

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586071del , CM000667.2:g.145586071del GRCh38
NC_000005.9:g.144965634del , CM000667.1:g.144965634del GRCh37
NC_000005.8:g.144945827del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112753del
XR_944308.1:n.662+178863del