Canonical Allele Identifier: CA25761355
Gene: DNASE2B HGNC NCBI

Linked Data

dbSNP Id: rs934738383
gnomAD v3: 1-84399467-C-T
gnomAD v4: 1-84399467-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84399467C>T , CM000663.2:g.84399467C>T GRCh38
NC_000001.10:g.84865150C>T , CM000663.1:g.84865150C>T GRCh37
NC_000001.9:g.84637738C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000370665.4:c.125+778C>T MANE Select ENSP00000359699.3:n.125+778C>T
ENST00000370665.3:c.125+778C>T ENSP00000359699.3:n.125+778C>T
NM_021233.2:c.125+778C>T NP_067056.2:n.125+778C>T
NM_021233.3:c.125+778C>T MANE Select NP_067056.2:n.125+778C>T