Canonical Allele Identifier: CA1969296587

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234861T= , CM000673.2:g.47234861T=	GRCh38
NC_000011.9:g.47256412T= , CM000673.1:g.47256412T=	GRCh37
NC_000011.8:g.47212988T=	NCBI36
NG_009365.1:g.24920T= , LRG_467:g.24920T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.807T= MANE Select	ENSP00000256996.4:p.Ile269=
ENST00000256996.8:c.807T=	ENSP00000256996.3:p.Ile269=
ENST00000378600.7:c.457-2976T=	ENSP00000367863.3:n.457-2976T=
ENST00000378601.7:c.702+189T=	ENSP00000367864.3:n.702+189T=
ENST00000378603.7:c.615T=	ENSP00000367866.3:p.Ile205=
ENST00000612309.4:n.1921T=
ENST00000614394.1:n.197T=
ENST00000616278.4:c.556+189T=	ENSP00000478411.1:n.556+189T=
ENST00000617022.4:n.1554-2976T=
ENST00000617847.4:c.736T=
ENST00000620515.1:n.46+189T=
NM_000107.2:c.807T= , LRG_467t1:c.807T=	NP_000098.1:p.Ile269=
NM_001300734.1:c.457-2976T=	NP_001287663.1:n.457-2976T=
XR_242780.3:n.870+189T=
XR_242780.4:n.870+189T=
NM_000107.3:c.807T= MANE Select	NP_000098.1:p.Ile269=
NM_001300734.2:c.457-2976T=	NP_001287663.1:n.457-2976T=
NM_001399874.1:c.807T=	NP_001386803.1:p.Ile269=
NM_001399875.1:c.807T=	NP_001386804.1:p.Ile269=
NM_001399876.1:c.457-2976T=	NP_001386805.1:n.457-2976T=
NM_001399878.1:c.615T=	NP_001386807.1:p.Ile205=
NR_174610.1:n.1131+189T=
NR_174611.1:n.1094T=