Canonical Allele Identifier: CA739693936

Gene: DNASE2B

Linked Data

• dbSNP Id: rs1224002663
• MyVariant Identifiers: chr1:g.84865685del (hg19) ; chr1:g.84400002del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84400004del , CM000663.2:g.84400004del	GRCh38
NC_000001.10:g.84865687del , CM000663.1:g.84865687del	GRCh37
NC_000001.9:g.84638275del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370665.4:c.125+1315del MANE Select	ENSP00000359699.3:n.125+1315del
ENST00000370665.3:c.125+1315del	ENSP00000359699.3:n.125+1315del
NM_021233.2:c.125+1315del	NP_067056.2:n.125+1315del
NM_021233.3:c.125+1315del MANE Select	NP_067056.2:n.125+1315del