Canonical Allele Identifier: CA380296309

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256446T>C (hg19) ; chr11:g.47234895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234895T>C , CM000673.2:g.47234895T>C	GRCh38
NC_000011.9:g.47256446T>C , CM000673.1:g.47256446T>C	GRCh37
NC_000011.8:g.47213022T>C	NCBI36
NG_009365.1:g.24954T>C , LRG_467:g.24954T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.841T>C MANE Select	ENSP00000256996.4:p.Phe281Leu
ENST00000256996.8:c.841T>C	ENSP00000256996.3:p.Phe281Leu
ENST00000378600.7:c.457-2942T>C	ENSP00000367863.3:n.457-2942T>C
ENST00000378601.7:c.702+223T>C	ENSP00000367864.3:n.702+223T>C
ENST00000378603.7:c.649T>C	ENSP00000367866.3:p.Phe217Leu
ENST00000612309.4:n.1955T>C
ENST00000614394.1:n.231T>C
ENST00000616278.4:c.556+223T>C	ENSP00000478411.1:n.556+223T>C
ENST00000617022.4:n.1554-2942T>C
ENST00000617847.4:c.770T>C
ENST00000620515.1:n.46+223T>C
NM_000107.2:c.841T>C , LRG_467t1:c.841T>C	NP_000098.1:p.Phe281Leu
NM_001300734.1:c.457-2942T>C	NP_001287663.1:n.457-2942T>C
XR_242780.3:n.870+223T>C
XR_242780.4:n.870+223T>C
NM_000107.3:c.841T>C MANE Select	NP_000098.1:p.Phe281Leu
NM_001300734.2:c.457-2942T>C	NP_001287663.1:n.457-2942T>C
NM_001399874.1:c.841T>C	NP_001386803.1:p.Phe281Leu
NM_001399875.1:c.841T>C	NP_001386804.1:p.Phe281Leu
NM_001399876.1:c.457-2942T>C	NP_001386805.1:n.457-2942T>C
NM_001399878.1:c.649T>C	NP_001386807.1:p.Phe217Leu
NR_174610.1:n.1131+223T>C
NR_174611.1:n.1109+19T>C