Canonical Allele Identifier: CA406714553
Gene: DBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48633485T>A , CM000681.2:g.48633485T>A GRCh38
NC_000019.9:g.49136742T>A , CM000681.1:g.49136742T>A GRCh37
NC_000019.8:g.53828554T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000222122.10:c.721A>T MANE Select ENSP00000222122.4:p.Met241Leu
ENST00000222122.9:c.721A>T ENSP00000222122.4:p.Met241Leu
ENST00000593500.1:c.115A>T ENSP00000471220.1:p.Met39Leu
ENST00000594723.1:n.2964A>T
ENST00000599385.5:c.115A>T ENSP00000469426.1:p.Met39Leu
ENST00000601104.1:c.721A>T ENSP00000469291.1:p.Met241Leu
NM_001352.4:c.721A>T NP_001343.2:p.Met241Leu
XM_017026388.2:c.292A>T XP_016881877.1:p.Met98Leu
XR_243907.4:n.1626A>T
NM_001352.5:c.721A>T MANE Select NP_001343.2:p.Met241Leu