Canonical Allele Identifier: CA5972655
Gene: DDB2 HGNC NCBI

Linked Data

dbSNP Id: rs761699363

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235294G>C , CM000673.2:g.47235294G>C GRCh38
NC_000011.9:g.47256845G>C , CM000673.1:g.47256845G>C GRCh37
NC_000011.8:g.47213421G>C NCBI36
NG_009365.1:g.25353G>C , LRG_467:g.25353G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.905G>C MANE Select ENSP00000256996.4:p.Arg302Pro
ENST00000256996.8:c.905G>C ENSP00000256996.3:p.Arg302Pro
ENST00000378600.7:c.457-2543G>C ENSP00000367863.3:n.457-2543G>C
ENST00000378601.7:c.727G>C ENSP00000367864.3:p.Gly243Arg
ENST00000378603.7:c.713G>C ENSP00000367866.3:p.Arg238Pro
ENST00000612309.4:n.2354G>C
ENST00000614394.1:n.295G>C
ENST00000616278.4:c.581G>C ENSP00000478411.1:n.581G>C
ENST00000617022.4:n.1554-2543G>C
ENST00000617847.4:c.834G>C
ENST00000620515.1:n.71G>C
NM_000107.2:c.905G>C , LRG_467t1:c.905G>C NP_000098.1:p.Arg302Pro
NM_001300734.1:c.457-2543G>C NP_001287663.1:n.457-2543G>C
XR_242780.3:n.895G>C
XR_242780.4:n.895G>C
NM_000107.3:c.905G>C MANE Select NP_000098.1:p.Arg302Pro
NM_001300734.2:c.457-2543G>C NP_001287663.1:n.457-2543G>C
NM_001399874.1:c.905G>C NP_001386803.1:p.Arg302Pro
NM_001399875.1:c.905G>C NP_001386804.1:p.Arg302Pro
NM_001399876.1:c.457-2543G>C NP_001386805.1:n.457-2543G>C
NM_001399878.1:c.713G>C NP_001386807.1:p.Arg238Pro
NR_174610.1:n.1156G>C
NR_174611.1:n.1134G>C