Canonical Allele Identifier: CA1144845770
Gene: DNASE2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399801T= , CM000663.2:g.84399801T= GRCh38
NC_000001.10:g.84865484T= , CM000663.1:g.84865484T= GRCh37
NC_000001.9:g.84638072T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1112T= MANE Select ENSP00000359699.3:n.125+1112T=
ENST00000370665.3:c.125+1112T= ENSP00000359699.3:n.125+1112T=
NM_021233.2:c.125+1112T= NP_067056.2:n.125+1112T=
NM_021233.3:c.125+1112T= MANE Select NP_067056.2:n.125+1112T=
Search 100 bp 5'
Search 100 bp 3'