Canonical Allele Identifier: CA2475662104
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs1680371877

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399618C>T , CM000663.2:g.84399618C>T GRCh38
NC_000001.10:g.84865301C>T , CM000663.1:g.84865301C>T GRCh37
NC_000001.9:g.84637889C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+929C>T MANE Select ENSP00000359699.3:n.125+929C>T
ENST00000370665.3:c.125+929C>T ENSP00000359699.3:n.125+929C>T
NM_021233.2:c.125+929C>T NP_067056.2:n.125+929C>T
NM_021233.3:c.125+929C>T MANE Select NP_067056.2:n.125+929C>T