Canonical Allele Identifier: CA1969297115

Gene: DDB2

Genomic Alleles

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

Transcript Alleles

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