Canonical Allele Identifier: CA406714436

Gene: DBP

Linked Data

• MyVariant Identifiers: chr19:g.49136693C>A (hg19) ; chr19:g.48633436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633436C>A , CM000681.2:g.48633436C>A	GRCh38
NC_000019.9:g.49136693C>A , CM000681.1:g.49136693C>A	GRCh37
NC_000019.8:g.53828505C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+8G>T MANE Select	ENSP00000222122.4:n.762+8G>T
ENST00000222122.9:c.762+8G>T	ENSP00000222122.4:n.762+8G>T
ENST00000593500.1:c.156+8G>T	ENSP00000471220.1:n.156+8G>T
ENST00000594723.1:n.3013G>T
ENST00000599385.5:c.156+8G>T	ENSP00000469426.1:n.156+8G>T
ENST00000601104.1:c.770G>T	ENSP00000469291.1:p.Arg257Ile
NM_001352.4:c.762+8G>T	NP_001343.2:n.762+8G>T
XM_017026388.2:c.333+8G>T	XP_016881877.1:n.333+8G>T
XR_243907.4:n.1667+8G>T
NM_001352.5:c.762+8G>T MANE Select	NP_001343.2:n.762+8G>T