Canonical Allele Identifier: CA1003913825
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1680364126
gnomAD v3: 1-84399549-G-T
gnomAD v4: 1-84399549-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399549G>T , CM000663.2:g.84399549G>T GRCh38
NC_000001.10:g.84865232G>T , CM000663.1:g.84865232G>T GRCh37
NC_000001.9:g.84637820G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+860G>T MANE Select ENSP00000359699.3:n.125+860G>T
ENST00000370665.3:c.125+860G>T ENSP00000359699.3:n.125+860G>T
NM_021233.2:c.125+860G>T NP_067056.2:n.125+860G>T
NM_021233.3:c.125+860G>T MANE Select NP_067056.2:n.125+860G>T
Search 100 bp 5'
Search 100 bp 3'