Canonical Allele Identifier: CA883024094

Gene: DBP

Linked Data

• dbSNP Id: rs1333823505
• gnomAD v4: 19-48633432-A-T
• MyVariant Identifiers: chr19:g.49136689A>T (hg19) ; chr19:g.48633432A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633432A>T , CM000681.2:g.48633432A>T	GRCh38
NC_000019.9:g.49136689A>T , CM000681.1:g.49136689A>T	GRCh37
NC_000019.8:g.53828501A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+12T>A MANE Select	ENSP00000222122.4:n.762+12T>A
ENST00000222122.9:c.762+12T>A	ENSP00000222122.4:n.762+12T>A
ENST00000593500.1:c.156+12T>A	ENSP00000471220.1:n.156+12T>A
ENST00000594723.1:n.3017T>A
ENST00000599385.5:c.156+12T>A	ENSP00000469426.1:n.156+12T>A
ENST00000601104.1:c.774T>A	ENSP00000469291.1:p.Ala258=
NM_001352.4:c.762+12T>A	NP_001343.2:n.762+12T>A
XM_017026388.2:c.333+12T>A	XP_016881877.1:n.333+12T>A
XR_243907.4:n.1667+12T>A
NM_001352.5:c.762+12T>A MANE Select	NP_001343.2:n.762+12T>A