Canonical Allele Identifier: CA508271106

Gene: DBP

Linked Data

• MyVariant Identifiers: chr19:g.49136746T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48633489T>C , CM000681.2:g.48633489T>C	GRCh38
NC_000019.9:g.49136746T>C , CM000681.1:g.49136746T>C	GRCh37
NC_000019.8:g.53828558T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222122.10:c.717A>G MANE Select	ENSP00000222122.4:p.Pro239=
ENST00000222122.9:c.717A>G	ENSP00000222122.4:p.Pro239=
ENST00000593500.1:c.111A>G	ENSP00000471220.1:p.Pro37=
ENST00000594723.1:n.2960A>G
ENST00000599385.5:c.111A>G	ENSP00000469426.1:p.Pro37=
ENST00000601104.1:c.717A>G	ENSP00000469291.1:p.Pro239=
NM_001352.4:c.717A>G	NP_001343.2:p.Pro239=
XM_017026388.2:c.288A>G	XP_016881877.1:p.Pro96=
XR_243907.4:n.1622A>G
NM_001352.5:c.717A>G MANE Select	NP_001343.2:p.Pro239=