Canonical Allele Identifier: CA1969296616

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234892A= , CM000673.2:g.47234892A=	GRCh38
NC_000011.9:g.47256443A= , CM000673.1:g.47256443A=	GRCh37
NC_000011.8:g.47213019A=	NCBI36
NG_009365.1:g.24951A= , LRG_467:g.24951A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.838A= MANE Select	ENSP00000256996.4:p.Ser280=
ENST00000256996.8:c.838A=	ENSP00000256996.3:p.Ser280=
ENST00000378600.7:c.457-2945A=	ENSP00000367863.3:n.457-2945A=
ENST00000378601.7:c.702+220A=	ENSP00000367864.3:n.702+220A=
ENST00000378603.7:c.646A=	ENSP00000367866.3:p.Ser216=
ENST00000612309.4:n.1952A=
ENST00000614394.1:n.228A=
ENST00000616278.4:c.556+220A=	ENSP00000478411.1:n.556+220A=
ENST00000617022.4:n.1554-2945A=
ENST00000617847.4:c.767A=
ENST00000620515.1:n.46+220A=
NM_000107.2:c.838A= , LRG_467t1:c.838A=	NP_000098.1:p.Ser280=
NM_001300734.1:c.457-2945A=	NP_001287663.1:n.457-2945A=
XR_242780.3:n.870+220A=
XR_242780.4:n.870+220A=
NM_000107.3:c.838A= MANE Select	NP_000098.1:p.Ser280=
NM_001300734.2:c.457-2945A=	NP_001287663.1:n.457-2945A=
NM_001399874.1:c.838A=	NP_001386803.1:p.Ser280=
NM_001399875.1:c.838A=	NP_001386804.1:p.Ser280=
NM_001399876.1:c.457-2945A=	NP_001386805.1:n.457-2945A=
NM_001399878.1:c.646A=	NP_001386807.1:p.Ser216=
NR_174610.1:n.1131+220A=
NR_174611.1:n.1109+16A=