Canonical Allele Identifier: CA1969297219
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235529G= , CM000673.2:g.47235529G= GRCh38
NC_000011.9:g.47257080G= , CM000673.1:g.47257080G= GRCh37
NC_000011.8:g.47213656G= NCBI36
NG_009365.1:g.25588G= , LRG_467:g.25588G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.1023+117G= MANE Select ENSP00000256996.4:n.1023+117G=
ENST00000256996.8:c.1023+117G= ENSP00000256996.3:n.1023+117G=
ENST00000378600.7:c.457-2308G= ENSP00000367863.3:n.457-2308G=
ENST00000378601.7:c.*110+117G= ENSP00000367864.3:n.*110+117G=
ENST00000378603.7:c.831+117G= ENSP00000367866.3:n.831+117G=
ENST00000612309.4:n.2472+117G=
ENST00000614394.1:n.530G=
ENST00000616278.4:c.699+117G= ENSP00000478411.1:n.699+117G=
ENST00000617022.4:n.1554-2308G=
ENST00000617847.4:c.952+117G=
ENST00000620515.1:n.189+117G=
NM_000107.2:c.1023+117G= , LRG_467t1:c.1023+117G= NP_000098.1:n.1023+117G=
NM_001300734.1:c.457-2308G= NP_001287663.1:n.457-2308G=
XR_242780.3:n.1013+117G=
XR_242780.4:n.1013+117G=
NM_000107.3:c.1023+117G= MANE Select NP_000098.1:n.1023+117G=
NM_001300734.2:c.457-2308G= NP_001287663.1:n.457-2308G=
NM_001399874.1:c.1023+117G= NP_001386803.1:n.1023+117G=
NM_001399875.1:c.1023+117G= NP_001386804.1:n.1023+117G=
NM_001399876.1:c.457-2308G= NP_001386805.1:n.457-2308G=
NM_001399878.1:c.831+117G= NP_001386807.1:n.831+117G=
NR_174610.1:n.1274+117G=
NR_174611.1:n.1252+117G=