Canonical Allele Identifier: CA474229283

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256936T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235385T>A , CM000673.2:g.47235385T>A	GRCh38
NC_000011.9:g.47256936T>A , CM000673.1:g.47256936T>A	GRCh37
NC_000011.8:g.47213512T>A	NCBI36
NG_009365.1:g.25444T>A , LRG_467:g.25444T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.996T>A MANE Select	ENSP00000256996.4:p.Arg332=
ENST00000256996.8:c.996T>A	ENSP00000256996.3:p.Arg332=
ENST00000378600.7:c.457-2452T>A	ENSP00000367863.3:n.457-2452T>A
ENST00000378601.7:c.*83T>A	ENSP00000367864.3:n.*83T>A
ENST00000378603.7:c.804T>A	ENSP00000367866.3:p.Arg268=
ENST00000612309.4:n.2445T>A
ENST00000614394.1:n.386T>A
ENST00000616278.4:c.672T>A	ENSP00000478411.1:n.672T>A
ENST00000617022.4:n.1554-2452T>A
ENST00000617847.4:c.925T>A
ENST00000620515.1:n.162T>A
NM_000107.2:c.996T>A , LRG_467t1:c.996T>A	NP_000098.1:p.Arg332=
NM_001300734.1:c.457-2452T>A	NP_001287663.1:n.457-2452T>A
XR_242780.3:n.986T>A
XR_242780.4:n.986T>A
NM_000107.3:c.996T>A MANE Select	NP_000098.1:p.Arg332=
NM_001300734.2:c.457-2452T>A	NP_001287663.1:n.457-2452T>A
NM_001399874.1:c.996T>A	NP_001386803.1:p.Arg332=
NM_001399875.1:c.996T>A	NP_001386804.1:p.Arg332=
NM_001399876.1:c.457-2452T>A	NP_001386805.1:n.457-2452T>A
NM_001399878.1:c.804T>A	NP_001386807.1:p.Arg268=
NR_174610.1:n.1247T>A
NR_174611.1:n.1225T>A