Canonical Allele Identifier: CA2475662255
Gene: DNASE2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84400002_84400005delinsAAAG , CM000663.2:g.84400002_84400005delinsAAAG GRCh38
NC_000001.10:g.84865685_84865688delinsAAAG , CM000663.1:g.84865685_84865688delinsAAAG GRCh37
NC_000001.9:g.84638273_84638276delinsAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1313_125+1316delinsAAAG MANE Select ENSP00000359699.3:n.125+1313_125+1316delinsAAAG
ENST00000370665.3:c.125+1313_125+1316delinsAAAG ENSP00000359699.3:n.125+1313_125+1316delinsAAAG
NM_021233.2:c.125+1313_125+1316delinsAAAG NP_067056.2:n.125+1313_125+1316delinsAAAG
NM_021233.3:c.125+1313_125+1316delinsAAAG MANE Select NP_067056.2:n.125+1313_125+1316delinsAAAG