Canonical Allele Identifier: CA739693707
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1173358637
MyVariant Identifiers: chr1:g.84865341C>T (hg19) chr1:g.84399658C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399658C>T , CM000663.2:g.84399658C>T GRCh38
NC_000001.10:g.84865341C>T , CM000663.1:g.84865341C>T GRCh37
NC_000001.9:g.84637929C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370665.4:c.125+969C>T MANE Select ENSP00000359699.3:n.125+969C>T
ENST00000370665.3:c.125+969C>T ENSP00000359699.3:n.125+969C>T
NM_021233.2:c.125+969C>T NP_067056.2:n.125+969C>T
NM_021233.3:c.125+969C>T MANE Select NP_067056.2:n.125+969C>T
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