Canonical Allele Identifier: CA25761351
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs552801224

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399459C>T , CM000663.2:g.84399459C>T GRCh38
NC_000001.10:g.84865142C>T , CM000663.1:g.84865142C>T GRCh37
NC_000001.9:g.84637730C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+770C>T MANE Select ENSP00000359699.3:n.125+770C>T
ENST00000370665.3:c.125+770C>T ENSP00000359699.3:n.125+770C>T
NM_021233.2:c.125+770C>T NP_067056.2:n.125+770C>T
NM_021233.3:c.125+770C>T MANE Select NP_067056.2:n.125+770C>T