Canonical Allele Identifier: CA2475662271
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1036490802
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84400028G>C , CM000663.2:g.84400028G>C GRCh38
NC_000001.10:g.84865711G>C , CM000663.1:g.84865711G>C GRCh37
NC_000001.9:g.84638299G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+1339G>C MANE Select ENSP00000359699.3:n.125+1339G>C
ENST00000370665.3:c.125+1339G>C ENSP00000359699.3:n.125+1339G>C
NM_021233.2:c.125+1339G>C NP_067056.2:n.125+1339G>C
NM_021233.3:c.125+1339G>C MANE Select NP_067056.2:n.125+1339G>C
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