Canonical Allele Identifier: CA406714435

Gene: DBP

Linked Data

• MyVariant Identifiers: chr19:g.49136692T>G (hg19) ; chr19:g.48633435T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633435T>G , CM000681.2:g.48633435T>G	GRCh38
NC_000019.9:g.49136692T>G , CM000681.1:g.49136692T>G	GRCh37
NC_000019.8:g.53828504T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.762+9A>C MANE Select	ENSP00000222122.4:n.762+9A>C
ENST00000222122.9:c.762+9A>C	ENSP00000222122.4:n.762+9A>C
ENST00000593500.1:c.156+9A>C	ENSP00000471220.1:n.156+9A>C
ENST00000594723.1:n.3014A>C
ENST00000599385.5:c.156+9A>C	ENSP00000469426.1:n.156+9A>C
ENST00000601104.1:c.771A>C	ENSP00000469291.1:p.Arg257Ser
NM_001352.4:c.762+9A>C	NP_001343.2:n.762+9A>C
XM_017026388.2:c.333+9A>C	XP_016881877.1:n.333+9A>C
XR_243907.4:n.1667+9A>C
NM_001352.5:c.762+9A>C MANE Select	NP_001343.2:n.762+9A>C