Canonical Allele Identifier: CA2339994923
Gene: DBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48633399G= , CM000681.2:g.48633399G= GRCh38
NC_000019.9:g.49136656G= , CM000681.1:g.49136656G= GRCh37
NC_000019.8:g.53828468G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000222122.10:c.762+45C= MANE Select ENSP00000222122.4:n.762+45C=
ENST00000222122.9:c.762+45C= ENSP00000222122.4:n.762+45C=
ENST00000593500.1:c.156+45C= ENSP00000471220.1:n.156+45C=
ENST00000594723.1:n.3050C=
ENST00000599385.5:c.156+45C= ENSP00000469426.1:n.156+45C=
ENST00000601104.1:c.*18C= ENSP00000469291.1:n.*18C=
NM_001352.4:c.762+45C= NP_001343.2:n.762+45C=
XM_017026388.2:c.333+45C= XP_016881877.1:n.333+45C=
XR_243907.4:n.1667+45C=
NM_001352.5:c.762+45C= MANE Select NP_001343.2:n.762+45C=
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