Canonical Allele Identifier: CA523776009
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1423960676
gnomAD v2: 1-84865417-AC-A
gnomAD v3: 1-84399734-AC-A
gnomAD v4: 1-84399734-AC-A
MyVariant Identifiers: chr1:g.84865418del (hg19) chr1:g.84399735del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399736del , CM000663.2:g.84399736del GRCh38
NC_000001.10:g.84865419del , CM000663.1:g.84865419del GRCh37
NC_000001.9:g.84638007del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1047del MANE Select ENSP00000359699.3:n.125+1047del
ENST00000370665.3:c.125+1047del ENSP00000359699.3:n.125+1047del
NM_021233.2:c.125+1047del NP_067056.2:n.125+1047del
NM_021233.3:c.125+1047del MANE Select NP_067056.2:n.125+1047del
Search 100 bp 5'
Search 100 bp 3'