Canonical Allele Identifier: CA1969296695

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234941T= , CM000673.2:g.47234941T=	GRCh38
NC_000011.9:g.47256492T= , CM000673.1:g.47256492T=	GRCh37
NC_000011.8:g.47213068T=	NCBI36
NG_009365.1:g.25000T= , LRG_467:g.25000T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+7T= MANE Select	ENSP00000256996.4:n.880+7T=
ENST00000256996.8:c.880+7T=	ENSP00000256996.3:n.880+7T=
ENST00000378600.7:c.457-2896T=	ENSP00000367863.3:n.457-2896T=
ENST00000378601.7:c.702+269T=	ENSP00000367864.3:n.702+269T=
ENST00000378603.7:c.688+7T=	ENSP00000367866.3:n.688+7T=
ENST00000612309.4:n.2001T=
ENST00000614394.1:n.270+7T=
ENST00000616278.4:c.556+269T=	ENSP00000478411.1:n.556+269T=
ENST00000617022.4:n.1554-2896T=
ENST00000617847.4:c.809+7T=
ENST00000620515.1:n.46+269T=
NM_000107.2:c.880+7T= , LRG_467t1:c.880+7T=	NP_000098.1:n.880+7T=
NM_001300734.1:c.457-2896T=	NP_001287663.1:n.457-2896T=
XR_242780.3:n.870+269T=
XR_242780.4:n.870+269T=
NM_000107.3:c.880+7T= MANE Select	NP_000098.1:n.880+7T=
NM_001300734.2:c.457-2896T=	NP_001287663.1:n.457-2896T=
NM_001399874.1:c.880+7T=	NP_001386803.1:n.880+7T=
NM_001399875.1:c.880+7T=	NP_001386804.1:n.880+7T=
NM_001399876.1:c.457-2896T=	NP_001386805.1:n.457-2896T=
NM_001399878.1:c.688+7T=	NP_001386807.1:n.688+7T=
NR_174610.1:n.1131+269T=
NR_174611.1:n.1109+65T=