Canonical Allele Identifier: CA2339994964
Gene: DBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48633465G= , CM000681.2:g.48633465G= GRCh38
NC_000019.9:g.49136722G= , CM000681.1:g.49136722G= GRCh37
NC_000019.8:g.53828534G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000222122.10:c.741C= MANE Select ENSP00000222122.4:p.Ile247=
ENST00000222122.9:c.741C= ENSP00000222122.4:p.Ile247=
ENST00000593500.1:c.135C= ENSP00000471220.1:p.Ile45=
ENST00000594723.1:n.2984C=
ENST00000599385.5:c.135C= ENSP00000469426.1:p.Ile45=
ENST00000601104.1:c.741C= ENSP00000469291.1:p.Ile247=
NM_001352.4:c.741C= NP_001343.2:p.Ile247=
XM_017026388.2:c.312C= XP_016881877.1:p.Ile104=
XR_243907.4:n.1646C=
NM_001352.5:c.741C= MANE Select NP_001343.2:p.Ile247=