Canonical Allele Identifier: CA25761410
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs987993058
gnomAD v3: 1-84399756-T-TG
gnomAD v4: 1-84399756-T-TG
MyVariant Identifiers: chr1:g.84865439_84865440insG (hg19) chr1:g.84399756_84399757insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399760dup , CM000663.2:g.84399760dup GRCh38
NC_000001.10:g.84865443dup , CM000663.1:g.84865443dup GRCh37
NC_000001.9:g.84638031dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1071dup MANE Select ENSP00000359699.3:n.125+1071dup
ENST00000370665.3:c.125+1071dup ENSP00000359699.3:n.125+1071dup
NM_021233.2:c.125+1071dup NP_067056.2:n.125+1071dup
NM_021233.3:c.125+1071dup MANE Select NP_067056.2:n.125+1071dup
Search 100 bp 5'
Search 100 bp 3'