Canonical Allele Identifier: CA633887922

Gene: DBP

Linked Data

• dbSNP Id: rs1260703003
• gnomAD v2: 19-49136659-T-G
• gnomAD v4: 19-48633402-T-G
• MyVariant Identifiers: chr19:g.49136659T>G (hg19) ; chr19:g.48633402T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633402T>G , CM000681.2:g.48633402T>G	GRCh38
NC_000019.9:g.49136659T>G , CM000681.1:g.49136659T>G	GRCh37
NC_000019.8:g.53828471T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000222122.10:c.762+42A>C MANE Select	ENSP00000222122.4:n.762+42A>C
ENST00000222122.9:c.762+42A>C	ENSP00000222122.4:n.762+42A>C
ENST00000593500.1:c.156+42A>C	ENSP00000471220.1:n.156+42A>C
ENST00000594723.1:n.3047A>C
ENST00000599385.5:c.156+42A>C	ENSP00000469426.1:n.156+42A>C
ENST00000601104.1:c.*15A>C	ENSP00000469291.1:n.*15A>C
NM_001352.4:c.762+42A>C	NP_001343.2:n.762+42A>C
XM_017026388.2:c.333+42A>C	XP_016881877.1:n.333+42A>C
XR_243907.4:n.1667+42A>C
NM_001352.5:c.762+42A>C MANE Select	NP_001343.2:n.762+42A>C