Canonical Allele Identifier: CA25761380
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs969489571
MyVariant Identifiers: chr1:g.84865260A>G (hg19) chr1:g.84399577A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399577A>G , CM000663.2:g.84399577A>G GRCh38
NC_000001.10:g.84865260A>G , CM000663.1:g.84865260A>G GRCh37
NC_000001.9:g.84637848A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+888A>G MANE Select ENSP00000359699.3:n.125+888A>G
ENST00000370665.3:c.125+888A>G ENSP00000359699.3:n.125+888A>G
NM_021233.2:c.125+888A>G NP_067056.2:n.125+888A>G
NM_021233.3:c.125+888A>G MANE Select NP_067056.2:n.125+888A>G
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