Canonical Allele Identifier: CA2475662050
Gene: DNASE2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399498A= , CM000663.2:g.84399498A= GRCh38
NC_000001.10:g.84865181A= , CM000663.1:g.84865181A= GRCh37
NC_000001.9:g.84637769A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+809A= MANE Select ENSP00000359699.3:n.125+809A=
ENST00000370665.3:c.125+809A= ENSP00000359699.3:n.125+809A=
NM_021233.2:c.125+809A= NP_067056.2:n.125+809A=
NM_021233.3:c.125+809A= MANE Select NP_067056.2:n.125+809A=