Canonical Allele Identifier: CA1969296650

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234913C= , CM000673.2:g.47234913C=	GRCh38
NC_000011.9:g.47256464C= , CM000673.1:g.47256464C=	GRCh37
NC_000011.8:g.47213040C=	NCBI36
NG_009365.1:g.24972C= , LRG_467:g.24972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.859C= MANE Select	ENSP00000256996.4:p.His287=
ENST00000256996.8:c.859C=	ENSP00000256996.3:p.His287=
ENST00000378600.7:c.457-2924C=	ENSP00000367863.3:n.457-2924C=
ENST00000378601.7:c.702+241C=	ENSP00000367864.3:n.702+241C=
ENST00000378603.7:c.667C=	ENSP00000367866.3:p.His223=
ENST00000612309.4:n.1973C=
ENST00000614394.1:n.249C=
ENST00000616278.4:c.556+241C=	ENSP00000478411.1:n.556+241C=
ENST00000617022.4:n.1554-2924C=
ENST00000617847.4:c.788C=
ENST00000620515.1:n.46+241C=
NM_000107.2:c.859C= , LRG_467t1:c.859C=	NP_000098.1:p.His287=
NM_001300734.1:c.457-2924C=	NP_001287663.1:n.457-2924C=
XR_242780.3:n.870+241C=
XR_242780.4:n.870+241C=
NM_000107.3:c.859C= MANE Select	NP_000098.1:p.His287=
NM_001300734.2:c.457-2924C=	NP_001287663.1:n.457-2924C=
NM_001399874.1:c.859C=	NP_001386803.1:p.His287=
NM_001399875.1:c.859C=	NP_001386804.1:p.His287=
NM_001399876.1:c.457-2924C=	NP_001386805.1:n.457-2924C=
NM_001399878.1:c.667C=	NP_001386807.1:p.His223=
NR_174610.1:n.1131+241C=
NR_174611.1:n.1109+37C=