Canonical Allele Identifier: CA446993901
Gene: PRELID2 HGNC NCBI

Linked Data

dbSNP Id: rs1561511011

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.145586034_145586036del , CM000667.2:g.145586034_145586036del GRCh38
NC_000005.9:g.144965597_144965599del , CM000667.1:g.144965597_144965599del GRCh37
NC_000005.8:g.144945790_144945792del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510259.5:n.71-112718_71-112716del
XR_944308.1:n.662+178898_662+178900del