Canonical Allele Identifier: CA25761378
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs950376339
gnomAD v2: 1-84865247-C-G
gnomAD v3: 1-84399564-C-G
gnomAD v4: 1-84399564-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399564C>G , CM000663.2:g.84399564C>G GRCh38
NC_000001.10:g.84865247C>G , CM000663.1:g.84865247C>G GRCh37
NC_000001.9:g.84637835C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+875C>G MANE Select ENSP00000359699.3:n.125+875C>G
ENST00000370665.3:c.125+875C>G ENSP00000359699.3:n.125+875C>G
NM_021233.2:c.125+875C>G NP_067056.2:n.125+875C>G
NM_021233.3:c.125+875C>G MANE Select NP_067056.2:n.125+875C>G