Canonical Allele Identifier: CA2339994928

Gene: DBP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633403G= , CM000681.2:g.48633403G=	GRCh38
NC_000019.9:g.49136660G= , CM000681.1:g.49136660G=	GRCh37
NC_000019.8:g.53828472G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+41C= MANE Select	ENSP00000222122.4:n.762+41C=
ENST00000222122.9:c.762+41C=	ENSP00000222122.4:n.762+41C=
ENST00000593500.1:c.156+41C=	ENSP00000471220.1:n.156+41C=
ENST00000594723.1:n.3046C=
ENST00000599385.5:c.156+41C=	ENSP00000469426.1:n.156+41C=
ENST00000601104.1:c.*14C=	ENSP00000469291.1:n.*14C=
NM_001352.4:c.762+41C=	NP_001343.2:n.762+41C=
XM_017026388.2:c.333+41C=	XP_016881877.1:n.333+41C=
XR_243907.4:n.1667+41C=
NM_001352.5:c.762+41C= MANE Select	NP_001343.2:n.762+41C=