Canonical Allele Identifier: CA2339994902

Gene: DBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633359C= , CM000681.2:g.48633359C=	GRCh38
NC_000019.9:g.49136616C= , CM000681.1:g.49136616C=	GRCh37
NC_000019.8:g.53828428C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+85G= MANE Select	ENSP00000222122.4:n.762+85G=
ENST00000222122.9:c.762+85G=	ENSP00000222122.4:n.762+85G=
ENST00000593500.1:c.156+85G=	ENSP00000471220.1:n.156+85G=
ENST00000594723.1:n.3090G=
ENST00000599385.5:c.156+85G=	ENSP00000469426.1:n.156+85G=
ENST00000601104.1:c.*58G=	ENSP00000469291.1:n.*58G=
NM_001352.4:c.762+85G=	NP_001343.2:n.762+85G=
XM_017026388.2:c.333+85G=	XP_016881877.1:n.333+85G=
XR_243907.4:n.1667+85G=
NM_001352.5:c.762+85G= MANE Select	NP_001343.2:n.762+85G=