Canonical Allele Identifier: CA1969297069

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235347T= , CM000673.2:g.47235347T=	GRCh38
NC_000011.9:g.47256898T= , CM000673.1:g.47256898T=	GRCh37
NC_000011.8:g.47213474T=	NCBI36
NG_009365.1:g.25406T= , LRG_467:g.25406T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.958T= MANE Select	ENSP00000256996.4:p.Trp320=
ENST00000256996.8:c.958T=	ENSP00000256996.3:p.Trp320=
ENST00000378600.7:c.457-2490T=	ENSP00000367863.3:n.457-2490T=
ENST00000378601.7:c.*45T=	ENSP00000367864.3:n.*45T=
ENST00000378603.7:c.766T=	ENSP00000367866.3:p.Trp256=
ENST00000612309.4:n.2407T=
ENST00000614394.1:n.348T=
ENST00000616278.4:c.634T=	ENSP00000478411.1:n.634T=
ENST00000617022.4:n.1554-2490T=
ENST00000617847.4:c.887T=
ENST00000620515.1:n.124T=
NM_000107.2:c.958T= , LRG_467t1:c.958T=	NP_000098.1:p.Trp320=
NM_001300734.1:c.457-2490T=	NP_001287663.1:n.457-2490T=
XR_242780.3:n.948T=
XR_242780.4:n.948T=
NM_000107.3:c.958T= MANE Select	NP_000098.1:p.Trp320=
NM_001300734.2:c.457-2490T=	NP_001287663.1:n.457-2490T=
NM_001399874.1:c.958T=	NP_001386803.1:p.Trp320=
NM_001399875.1:c.958T=	NP_001386804.1:p.Trp320=
NM_001399876.1:c.457-2490T=	NP_001386805.1:n.457-2490T=
NM_001399878.1:c.766T=	NP_001386807.1:p.Trp256=
NR_174610.1:n.1209T=
NR_174611.1:n.1187T=