Canonical Allele Identifier: CA677042844
Gene: DDB2 HGNC NCBI

Linked Data

dbSNP Id: rs1448233555

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235080_47235085dup , CM000673.2:g.47235080_47235085dup GRCh38
NC_000011.9:g.47256631_47256636dup , CM000673.1:g.47256631_47256636dup GRCh37
NC_000011.8:g.47213207_47213212dup NCBI36
NG_009365.1:g.25139_25144dup , LRG_467:g.25139_25144dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.880+146_880+151dup MANE Select ENSP00000256996.4:n.880+146_880+151dup
ENST00000256996.8:c.880+146_880+151dup ENSP00000256996.3:n.880+146_880+151dup
ENST00000378600.7:c.457-2757_457-2752dup ENSP00000367863.3:n.457-2757_457-2752dup
ENST00000378601.7:c.703-190_703-185dup ENSP00000367864.3:n.703-190_703-185dup
ENST00000378603.7:c.688+146_688+151dup ENSP00000367866.3:n.688+146_688+151dup
ENST00000612309.4:n.2140_2145dup
ENST00000614394.1:n.270+146_270+151dup
ENST00000616278.4:c.557-190_557-185dup ENSP00000478411.1:n.557-190_557-185dup
ENST00000617022.4:n.1554-2757_1554-2752dup
ENST00000617847.4:c.809+146_809+151dup
ENST00000620515.1:n.47-190_47-185dup
NM_000107.2:c.880+146_880+151dup , LRG_467t1:c.880+146_880+151dup NP_000098.1:n.880+146_880+151dup
NM_001300734.1:c.457-2757_457-2752dup NP_001287663.1:n.457-2757_457-2752dup
XR_242780.3:n.871-190_871-185dup
XR_242780.4:n.871-190_871-185dup
NM_000107.3:c.880+146_880+151dup MANE Select NP_000098.1:n.880+146_880+151dup
NM_001300734.2:c.457-2757_457-2752dup NP_001287663.1:n.457-2757_457-2752dup
NM_001399874.1:c.880+146_880+151dup NP_001386803.1:n.880+146_880+151dup
NM_001399875.1:c.880+146_880+151dup NP_001386804.1:n.880+146_880+151dup
NM_001399876.1:c.457-2757_457-2752dup NP_001386805.1:n.457-2757_457-2752dup
NM_001399878.1:c.688+146_688+151dup NP_001386807.1:n.688+146_688+151dup
NR_174610.1:n.1132-190_1132-185dup
NR_174611.1:n.1110-190_1110-185dup