Canonical Allele Identifier: CA2475662113
Gene: DNASE2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399640A= , CM000663.2:g.84399640A= GRCh38
NC_000001.10:g.84865323A= , CM000663.1:g.84865323A= GRCh37
NC_000001.9:g.84637911A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+951A= MANE Select ENSP00000359699.3:n.125+951A=
ENST00000370665.3:c.125+951A= ENSP00000359699.3:n.125+951A=
NM_021233.2:c.125+951A= NP_067056.2:n.125+951A=
NM_021233.3:c.125+951A= MANE Select NP_067056.2:n.125+951A=
Search 100 bp 5'
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