Canonical Allele Identifier: CA2475662032
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1570297335
gnomAD v3: 1-84399460-A-G
gnomAD v4: 1-84399460-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399460A>G , CM000663.2:g.84399460A>G GRCh38
NC_000001.10:g.84865143A>G , CM000663.1:g.84865143A>G GRCh37
NC_000001.9:g.84637731A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+771A>G MANE Select ENSP00000359699.3:n.125+771A>G
ENST00000370665.3:c.125+771A>G ENSP00000359699.3:n.125+771A>G
NM_021233.2:c.125+771A>G NP_067056.2:n.125+771A>G
NM_021233.3:c.125+771A>G MANE Select NP_067056.2:n.125+771A>G
Search 100 bp 5'
Search 100 bp 3'