Canonical Allele Identifier: CA1969297077

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235354G= , CM000673.2:g.47235354G=	GRCh38
NC_000011.9:g.47256905G= , CM000673.1:g.47256905G=	GRCh37
NC_000011.8:g.47213481G=	NCBI36
NG_009365.1:g.25413G= , LRG_467:g.25413G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.965G= MANE Select	ENSP00000256996.4:p.Cys322=
ENST00000256996.8:c.965G=	ENSP00000256996.3:p.Cys322=
ENST00000378600.7:c.457-2483G=	ENSP00000367863.3:n.457-2483G=
ENST00000378601.7:c.*52G=	ENSP00000367864.3:n.*52G=
ENST00000378603.7:c.773G=	ENSP00000367866.3:p.Cys258=
ENST00000612309.4:n.2414G=
ENST00000614394.1:n.355G=
ENST00000616278.4:c.641G=	ENSP00000478411.1:n.641G=
ENST00000617022.4:n.1554-2483G=
ENST00000617847.4:c.894G=
ENST00000620515.1:n.131G=
NM_000107.2:c.965G= , LRG_467t1:c.965G=	NP_000098.1:p.Cys322=
NM_001300734.1:c.457-2483G=	NP_001287663.1:n.457-2483G=
XR_242780.3:n.955G=
XR_242780.4:n.955G=
NM_000107.3:c.965G= MANE Select	NP_000098.1:p.Cys322=
NM_001300734.2:c.457-2483G=	NP_001287663.1:n.457-2483G=
NM_001399874.1:c.965G=	NP_001386803.1:p.Cys322=
NM_001399875.1:c.965G=	NP_001386804.1:p.Cys322=
NM_001399876.1:c.457-2483G=	NP_001386805.1:n.457-2483G=
NM_001399878.1:c.773G=	NP_001386807.1:p.Cys258=
NR_174610.1:n.1216G=
NR_174611.1:n.1194G=