Canonical Allele Identifier: CA406714466

Gene: DBP

Linked Data

• MyVariant Identifiers: chr19:g.49136705T>C (hg19) ; chr19:g.48633448T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633448T>C , CM000681.2:g.48633448T>C	GRCh38
NC_000019.9:g.49136705T>C , CM000681.1:g.49136705T>C	GRCh37
NC_000019.8:g.53828517T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.758A>G MANE Select	ENSP00000222122.4:p.Gln253Arg
ENST00000222122.9:c.758A>G	ENSP00000222122.4:p.Gln253Arg
ENST00000593500.1:c.152A>G	ENSP00000471220.1:p.Gln51Arg
ENST00000594723.1:n.3001A>G
ENST00000599385.5:c.152A>G	ENSP00000469426.1:p.Gln51Arg
ENST00000601104.1:c.758A>G	ENSP00000469291.1:p.Gln253Arg
NM_001352.4:c.758A>G	NP_001343.2:p.Gln253Arg
XM_017026388.2:c.329A>G	XP_016881877.1:p.Gln110Arg
XR_243907.4:n.1663A>G
NM_001352.5:c.758A>G MANE Select	NP_001343.2:p.Gln253Arg