Canonical Allele Identifier: CA380298564
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47238799G>A , CM000673.2:g.47238799G>A GRCh38
NC_000011.9:g.47260350G>A , CM000673.1:g.47260350G>A GRCh37
NC_000011.8:g.47216926G>A NCBI36
NG_009365.1:g.28858G>A , LRG_467:g.28858G>A
NG_023296.1:g.15108C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.1235-1G>A MANE Select ENSP00000256996.4:n.1235-1G>A
ENST00000256996.8:c.1235-1G>A ENSP00000256996.3:n.1235-1G>A
ENST00000378600.7:c.668-1G>A ENSP00000367863.3:n.668-1G>A
ENST00000378601.7:c.*322-1G>A ENSP00000367864.3:n.*322-1G>A
ENST00000378603.7:c.1043-1G>A ENSP00000367866.3:n.1043-1G>A
ENST00000612309.4:n.2684-1G>A
ENST00000614884.1:n.243-1G>A
ENST00000616278.4:c.911-1G>A ENSP00000478411.1:n.911-1G>A
ENST00000617022.4:n.1765-1G>A
ENST00000617847.4:c.1258-1G>A
NM_000107.2:c.1235-1G>A , LRG_467t1:c.1235-1G>A NP_000098.1:n.1235-1G>A
NM_001300734.1:c.668-1G>A NP_001287663.1:n.668-1G>A
XR_242780.3:n.1225-1G>A
XR_242780.4:n.1225-1G>A
NM_000107.3:c.1235-1G>A MANE Select NP_000098.1:n.1235-1G>A
NM_001300734.2:c.668-1G>A NP_001287663.1:n.668-1G>A
NM_001399874.1:c.1235-1G>A NP_001386803.1:n.1235-1G>A
NM_001399875.1:c.1235-1G>A NP_001386804.1:n.1235-1G>A
NM_001399876.1:c.668-1G>A NP_001386805.1:n.668-1G>A
NM_001399878.1:c.1043-1G>A NP_001386807.1:n.1043-1G>A
NR_174610.1:n.1486-1G>A
NR_174611.1:n.1464-1G>A