Canonical Allele Identifier: CA739693645

Gene: DNASE2B

Linked Data

• dbSNP Id: rs1451055404
• gnomAD v3: 1-84399534-G-A
• gnomAD v4: 1-84399534-G-A
• MyVariant Identifiers: chr1:g.84865217G>A (hg19) ; chr1:g.84399534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84399534G>A , CM000663.2:g.84399534G>A	GRCh38
NC_000001.10:g.84865217G>A , CM000663.1:g.84865217G>A	GRCh37
NC_000001.9:g.84637805G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370665.4:c.125+845G>A MANE Select	ENSP00000359699.3:n.125+845G>A
ENST00000370665.3:c.125+845G>A	ENSP00000359699.3:n.125+845G>A
NM_021233.2:c.125+845G>A	NP_067056.2:n.125+845G>A
NM_021233.3:c.125+845G>A MANE Select	NP_067056.2:n.125+845G>A