Canonical Allele Identifier: CA1969296635

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234906G= , CM000673.2:g.47234906G=	GRCh38
NC_000011.9:g.47256457G= , CM000673.1:g.47256457G=	GRCh37
NC_000011.8:g.47213033G=	NCBI36
NG_009365.1:g.24965G= , LRG_467:g.24965G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.852G= MANE Select	ENSP00000256996.4:p.Ser284=
ENST00000256996.8:c.852G=	ENSP00000256996.3:p.Ser284=
ENST00000378600.7:c.457-2931G=	ENSP00000367863.3:n.457-2931G=
ENST00000378601.7:c.702+234G=	ENSP00000367864.3:n.702+234G=
ENST00000378603.7:c.660G=	ENSP00000367866.3:p.Ser220=
ENST00000612309.4:n.1966G=
ENST00000614394.1:n.242G=
ENST00000616278.4:c.556+234G=	ENSP00000478411.1:n.556+234G=
ENST00000617022.4:n.1554-2931G=
ENST00000617847.4:c.781G=
ENST00000620515.1:n.46+234G=
NM_000107.2:c.852G= , LRG_467t1:c.852G=	NP_000098.1:p.Ser284=
NM_001300734.1:c.457-2931G=	NP_001287663.1:n.457-2931G=
XR_242780.3:n.870+234G=
XR_242780.4:n.870+234G=
NM_000107.3:c.852G= MANE Select	NP_000098.1:p.Ser284=
NM_001300734.2:c.457-2931G=	NP_001287663.1:n.457-2931G=
NM_001399874.1:c.852G=	NP_001386803.1:p.Ser284=
NM_001399875.1:c.852G=	NP_001386804.1:p.Ser284=
NM_001399876.1:c.457-2931G=	NP_001386805.1:n.457-2931G=
NM_001399878.1:c.660G=	NP_001386807.1:p.Ser220=
NR_174610.1:n.1131+234G=
NR_174611.1:n.1109+30G=