Canonical Allele Identifier: CA474229262

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256909C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235358C>T , CM000673.2:g.47235358C>T	GRCh38
NC_000011.9:g.47256909C>T , CM000673.1:g.47256909C>T	GRCh37
NC_000011.8:g.47213485C>T	NCBI36
NG_009365.1:g.25417C>T , LRG_467:g.25417C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.969C>T MANE Select	ENSP00000256996.4:p.Pro323=
ENST00000256996.8:c.969C>T	ENSP00000256996.3:p.Pro323=
ENST00000378600.7:c.457-2479C>T	ENSP00000367863.3:n.457-2479C>T
ENST00000378601.7:c.*56C>T	ENSP00000367864.3:n.*56C>T
ENST00000378603.7:c.777C>T	ENSP00000367866.3:p.Pro259=
ENST00000612309.4:n.2418C>T
ENST00000614394.1:n.359C>T
ENST00000616278.4:c.645C>T	ENSP00000478411.1:n.645C>T
ENST00000617022.4:n.1554-2479C>T
ENST00000617847.4:c.898C>T
ENST00000620515.1:n.135C>T
NM_000107.2:c.969C>T , LRG_467t1:c.969C>T	NP_000098.1:p.Pro323=
NM_001300734.1:c.457-2479C>T	NP_001287663.1:n.457-2479C>T
XR_242780.3:n.959C>T
XR_242780.4:n.959C>T
NM_000107.3:c.969C>T MANE Select	NP_000098.1:p.Pro323=
NM_001300734.2:c.457-2479C>T	NP_001287663.1:n.457-2479C>T
NM_001399874.1:c.969C>T	NP_001386803.1:p.Pro323=
NM_001399875.1:c.969C>T	NP_001386804.1:p.Pro323=
NM_001399876.1:c.457-2479C>T	NP_001386805.1:n.457-2479C>T
NM_001399878.1:c.777C>T	NP_001386807.1:p.Pro259=
NR_174610.1:n.1220C>T
NR_174611.1:n.1198C>T