Canonical Allele Identifier: CA2475662211
Gene: DNASE2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399891_84399895delinsGGGCT , CM000663.2:g.84399891_84399895delinsGGGCT GRCh38
NC_000001.10:g.84865574_84865578delinsGGGCT , CM000663.1:g.84865574_84865578delinsGGGCT GRCh37
NC_000001.9:g.84638162_84638166delinsGGGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1202_125+1206delinsGGGCT MANE Select ENSP00000359699.3:n.125+1202_125+1206delinsGGGCT
ENST00000370665.3:c.125+1202_125+1206delinsGGGCT ENSP00000359699.3:n.125+1202_125+1206delinsGGGCT
NM_021233.2:c.125+1202_125+1206delinsGGGCT NP_067056.2:n.125+1202_125+1206delinsGGGCT
NM_021233.3:c.125+1202_125+1206delinsGGGCT MANE Select NP_067056.2:n.125+1202_125+1206delinsGGGCT