Canonical Allele Identifier: CA1003913808
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1680362164
gnomAD v3: 1-84399452-A-C
gnomAD v4: 1-84399452-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399452A>C , CM000663.2:g.84399452A>C GRCh38
NC_000001.10:g.84865135A>C , CM000663.1:g.84865135A>C GRCh37
NC_000001.9:g.84637723A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+763A>C MANE Select ENSP00000359699.3:n.125+763A>C
ENST00000370665.3:c.125+763A>C ENSP00000359699.3:n.125+763A>C
NM_021233.2:c.125+763A>C NP_067056.2:n.125+763A>C
NM_021233.3:c.125+763A>C MANE Select NP_067056.2:n.125+763A>C
Search 100 bp 5'
Search 100 bp 3'