Canonical Allele Identifier: CA9555074
Gene: DBP HGNC NCBI

Linked Data

dbSNP Id: rs201722098
ExAC: 19:49136655 G / T
gnomAD v2: 19-49136655-G-T
gnomAD v3: 19-48633398-G-T
gnomAD v4: 19-48633398-G-T
MyVariant Identifiers: chr19:g.49136655G>T (hg19) chr19:g.48633398G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48633398G>T , CM000681.2:g.48633398G>T GRCh38
NC_000019.9:g.49136655G>T , CM000681.1:g.49136655G>T GRCh37
NC_000019.8:g.53828467G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000222122.10:c.762+46C>A MANE Select ENSP00000222122.4:n.762+46C>A
ENST00000222122.9:c.762+46C>A ENSP00000222122.4:n.762+46C>A
ENST00000593500.1:c.156+46C>A ENSP00000471220.1:n.156+46C>A
ENST00000594723.1:n.3051C>A
ENST00000599385.5:c.156+46C>A ENSP00000469426.1:n.156+46C>A
ENST00000601104.1:c.*19C>A ENSP00000469291.1:n.*19C>A
NM_001352.4:c.762+46C>A NP_001343.2:n.762+46C>A
XM_017026388.2:c.333+46C>A XP_016881877.1:n.333+46C>A
XR_243907.4:n.1667+46C>A
NM_001352.5:c.762+46C>A MANE Select NP_001343.2:n.762+46C>A
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