Canonical Allele Identifier: CA2573496102
Gene: DNASE2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84400040C>G , CM000663.2:g.84400040C>G GRCh38
NC_000001.10:g.84865723C>G , CM000663.1:g.84865723C>G GRCh37
NC_000001.9:g.84638311C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1351C>G MANE Select ENSP00000359699.3:n.125+1351C>G
ENST00000370665.3:c.125+1351C>G ENSP00000359699.3:n.125+1351C>G
NM_021233.2:c.125+1351C>G NP_067056.2:n.125+1351C>G
NM_021233.3:c.125+1351C>G MANE Select NP_067056.2:n.125+1351C>G
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