Canonical Allele Identifier: CA474228735

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256403A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234852A>C , CM000673.2:g.47234852A>C	GRCh38
NC_000011.9:g.47256403A>C , CM000673.1:g.47256403A>C	GRCh37
NC_000011.8:g.47212979A>C	NCBI36
NG_009365.1:g.24911A>C , LRG_467:g.24911A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.798A>C MANE Select	ENSP00000256996.4:p.Thr266=
ENST00000256996.8:c.798A>C	ENSP00000256996.3:p.Thr266=
ENST00000378600.7:c.457-2985A>C	ENSP00000367863.3:n.457-2985A>C
ENST00000378601.7:c.702+180A>C	ENSP00000367864.3:n.702+180A>C
ENST00000378603.7:c.606A>C	ENSP00000367866.3:p.Thr202=
ENST00000612309.4:n.1912A>C
ENST00000614394.1:n.188A>C
ENST00000616278.4:c.556+180A>C	ENSP00000478411.1:n.556+180A>C
ENST00000617022.4:n.1554-2985A>C
ENST00000617847.4:c.727A>C
ENST00000620515.1:n.46+180A>C
NM_000107.2:c.798A>C , LRG_467t1:c.798A>C	NP_000098.1:p.Thr266=
NM_001300734.1:c.457-2985A>C	NP_001287663.1:n.457-2985A>C
XR_242780.3:n.870+180A>C
XR_242780.4:n.870+180A>C
NM_000107.3:c.798A>C MANE Select	NP_000098.1:p.Thr266=
NM_001300734.2:c.457-2985A>C	NP_001287663.1:n.457-2985A>C
NM_001399874.1:c.798A>C	NP_001386803.1:p.Thr266=
NM_001399875.1:c.798A>C	NP_001386804.1:p.Thr266=
NM_001399876.1:c.457-2985A>C	NP_001386805.1:n.457-2985A>C
NM_001399878.1:c.606A>C	NP_001386807.1:p.Thr202=
NR_174610.1:n.1131+180A>C
NR_174611.1:n.1085A>C