Canonical Allele Identifier: CA1969296699

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234942A= , CM000673.2:g.47234942A=	GRCh38
NC_000011.9:g.47256493A= , CM000673.1:g.47256493A=	GRCh37
NC_000011.8:g.47213069A=	NCBI36
NG_009365.1:g.25001A= , LRG_467:g.25001A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+8A= MANE Select	ENSP00000256996.4:n.880+8A=
ENST00000256996.8:c.880+8A=	ENSP00000256996.3:n.880+8A=
ENST00000378600.7:c.457-2895A=	ENSP00000367863.3:n.457-2895A=
ENST00000378601.7:c.702+270A=	ENSP00000367864.3:n.702+270A=
ENST00000378603.7:c.688+8A=	ENSP00000367866.3:n.688+8A=
ENST00000612309.4:n.2002A=
ENST00000614394.1:n.270+8A=
ENST00000616278.4:c.556+270A=	ENSP00000478411.1:n.556+270A=
ENST00000617022.4:n.1554-2895A=
ENST00000617847.4:c.809+8A=
ENST00000620515.1:n.46+270A=
NM_000107.2:c.880+8A= , LRG_467t1:c.880+8A=	NP_000098.1:n.880+8A=
NM_001300734.1:c.457-2895A=	NP_001287663.1:n.457-2895A=
XR_242780.3:n.870+270A=
XR_242780.4:n.870+270A=
NM_000107.3:c.880+8A= MANE Select	NP_000098.1:n.880+8A=
NM_001300734.2:c.457-2895A=	NP_001287663.1:n.457-2895A=
NM_001399874.1:c.880+8A=	NP_001386803.1:n.880+8A=
NM_001399875.1:c.880+8A=	NP_001386804.1:n.880+8A=
NM_001399876.1:c.457-2895A=	NP_001386805.1:n.457-2895A=
NM_001399878.1:c.688+8A=	NP_001386807.1:n.688+8A=
NR_174610.1:n.1131+270A=
NR_174611.1:n.1109+66A=