Canonical Allele Identifier: CA2586229396

Gene: DBP

Linked Data

• gnomAD v4: 19-48633352-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633352A>C , CM000681.2:g.48633352A>C	GRCh38
NC_000019.9:g.49136609A>C , CM000681.1:g.49136609A>C	GRCh37
NC_000019.8:g.53828421A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+92T>G MANE Select	ENSP00000222122.4:n.762+92T>G
ENST00000222122.9:c.762+92T>G	ENSP00000222122.4:n.762+92T>G
ENST00000593500.1:c.156+92T>G	ENSP00000471220.1:n.156+92T>G
ENST00000594723.1:n.3097T>G
ENST00000599385.5:c.156+92T>G	ENSP00000469426.1:n.156+92T>G
ENST00000601104.1:c.*65T>G	ENSP00000469291.1:n.*65T>G
NM_001352.4:c.762+92T>G	NP_001343.2:n.762+92T>G
XM_017026388.2:c.333+92T>G	XP_016881877.1:n.333+92T>G
XR_243907.4:n.1667+92T>G
NM_001352.5:c.762+92T>G MANE Select	NP_001343.2:n.762+92T>G