Canonical Allele Identifier: CA2475662108
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs576898756

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399630A>T , CM000663.2:g.84399630A>T GRCh38
NC_000001.10:g.84865313A>T , CM000663.1:g.84865313A>T GRCh37
NC_000001.9:g.84637901A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+941A>T MANE Select ENSP00000359699.3:n.125+941A>T
ENST00000370665.3:c.125+941A>T ENSP00000359699.3:n.125+941A>T
NM_021233.2:c.125+941A>T NP_067056.2:n.125+941A>T
NM_021233.3:c.125+941A>T MANE Select NP_067056.2:n.125+941A>T