Canonical Allele Identifier: CA1003913879
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1680377710
gnomAD v3: 1-84400004-AG-A
gnomAD v4: 1-84400004-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84400005del , CM000663.2:g.84400005del GRCh38
NC_000001.10:g.84865688del , CM000663.1:g.84865688del GRCh37
NC_000001.9:g.84638276del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1316del MANE Select ENSP00000359699.3:n.125+1316del
ENST00000370665.3:c.125+1316del ENSP00000359699.3:n.125+1316del
NM_021233.2:c.125+1316del NP_067056.2:n.125+1316del
NM_021233.3:c.125+1316del MANE Select NP_067056.2:n.125+1316del
Search 100 bp 5'
Search 100 bp 3'