Canonical Allele Identifier: CA25761363

Gene: DNASE2B

Linked Data

• dbSNP Id: rs190634985
• gnomAD v2: 1-84865204-A-G
• gnomAD v3: 1-84399521-A-G
• gnomAD v4: 1-84399521-A-G
• MyVariant Identifiers: chr1:g.84865204A>G (hg19) ; chr1:g.84399521A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84399521A>G , CM000663.2:g.84399521A>G	GRCh38
NC_000001.10:g.84865204A>G , CM000663.1:g.84865204A>G	GRCh37
NC_000001.9:g.84637792A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370665.4:c.125+832A>G MANE Select	ENSP00000359699.3:n.125+832A>G
ENST00000370665.3:c.125+832A>G	ENSP00000359699.3:n.125+832A>G
NM_021233.2:c.125+832A>G	NP_067056.2:n.125+832A>G
NM_021233.3:c.125+832A>G MANE Select	NP_067056.2:n.125+832A>G