Canonical Allele Identifier: CA1969296429

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234688T= , CM000673.2:g.47234688T=	GRCh38
NC_000011.9:g.47256239T= , CM000673.1:g.47256239T=	GRCh37
NC_000011.8:g.47212815T=	NCBI36
NG_009365.1:g.24747T= , LRG_467:g.24747T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000256996.9:c.702+16T= MANE Select	ENSP00000256996.4:n.702+16T=
ENST00000256996.8:c.702+16T=	ENSP00000256996.3:n.702+16T=
ENST00000378600.7:c.457-3149T=	ENSP00000367863.3:n.457-3149T=
ENST00000378601.7:c.702+16T=	ENSP00000367864.3:n.702+16T=
ENST00000378603.7:c.510+16T=	ENSP00000367866.3:n.510+16T=
ENST00000612309.4:n.1816+16T=
ENST00000614394.1:n.92+16T=
ENST00000616278.4:c.556+16T=	ENSP00000478411.1:n.556+16T=
ENST00000617022.4:n.1554-3149T=
ENST00000617847.4:c.631+16T=
ENST00000620515.1:n.46+16T=
NM_000107.2:c.702+16T= , LRG_467t1:c.702+16T=	NP_000098.1:n.702+16T=
NM_001300734.1:c.457-3149T=	NP_001287663.1:n.457-3149T=
XR_242780.3:n.870+16T=
XR_242780.4:n.870+16T=
NM_000107.3:c.702+16T= MANE Select	NP_000098.1:n.702+16T=
NM_001300734.2:c.457-3149T=	NP_001287663.1:n.457-3149T=
NM_001399874.1:c.702+16T=	NP_001386803.1:n.702+16T=
NM_001399875.1:c.702+16T=	NP_001386804.1:n.702+16T=
NM_001399876.1:c.457-3149T=	NP_001386805.1:n.457-3149T=
NM_001399878.1:c.510+16T=	NP_001386807.1:n.510+16T=
NR_174610.1:n.1131+16T=
NR_174611.1:n.989+16T=