Canonical Allele Identifier: CA1969296473
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47234725T= , CM000673.2:g.47234725T= GRCh38
NC_000011.9:g.47256276T= , CM000673.1:g.47256276T= GRCh37
NC_000011.8:g.47212852T= NCBI36
NG_009365.1:g.24784T= , LRG_467:g.24784T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.703-32T= MANE Select ENSP00000256996.4:n.703-32T=
ENST00000256996.8:c.703-32T= ENSP00000256996.3:n.703-32T=
ENST00000378600.7:c.457-3112T= ENSP00000367863.3:n.457-3112T=
ENST00000378601.7:c.702+53T= ENSP00000367864.3:n.702+53T=
ENST00000378603.7:c.511-32T= ENSP00000367866.3:n.511-32T=
ENST00000612309.4:n.1817-32T=
ENST00000614394.1:n.93-32T=
ENST00000616278.4:c.556+53T= ENSP00000478411.1:n.556+53T=
ENST00000617022.4:n.1554-3112T=
ENST00000617847.4:c.632-32T=
ENST00000620515.1:n.46+53T=
NM_000107.2:c.703-32T= , LRG_467t1:c.703-32T= NP_000098.1:n.703-32T=
NM_001300734.1:c.457-3112T= NP_001287663.1:n.457-3112T=
XR_242780.3:n.870+53T=
XR_242780.4:n.870+53T=
NM_000107.3:c.703-32T= MANE Select NP_000098.1:n.703-32T=
NM_001300734.2:c.457-3112T= NP_001287663.1:n.457-3112T=
NM_001399874.1:c.703-32T= NP_001386803.1:n.703-32T=
NM_001399875.1:c.703-32T= NP_001386804.1:n.703-32T=
NM_001399876.1:c.457-3112T= NP_001386805.1:n.457-3112T=
NM_001399878.1:c.511-32T= NP_001386807.1:n.511-32T=
NR_174610.1:n.1131+53T=
NR_174611.1:n.990-32T=