Canonical Allele Identifier: CA2475662163
Gene: DNASE2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399768_84399769delinsAG , CM000663.2:g.84399768_84399769delinsAG GRCh38
NC_000001.10:g.84865451_84865452delinsAG , CM000663.1:g.84865451_84865452delinsAG GRCh37
NC_000001.9:g.84638039_84638040delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1079_125+1080delinsAG MANE Select ENSP00000359699.3:n.125+1079_125+1080delinsAG
ENST00000370665.3:c.125+1079_125+1080delinsAG ENSP00000359699.3:n.125+1079_125+1080delinsAG
NM_021233.2:c.125+1079_125+1080delinsAG NP_067056.2:n.125+1079_125+1080delinsAG
NM_021233.3:c.125+1079_125+1080delinsAG MANE Select NP_067056.2:n.125+1079_125+1080delinsAG