Canonical Allele Identifier: CA380297210

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256953C>T (hg19) ; chr11:g.47235402C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235402C>T , CM000673.2:g.47235402C>T	GRCh38
NC_000011.9:g.47256953C>T , CM000673.1:g.47256953C>T	GRCh37
NC_000011.8:g.47213529C>T	NCBI36
NG_009365.1:g.25461C>T , LRG_467:g.25461C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.1013C>T MANE Select	ENSP00000256996.4:p.Thr338Ile
ENST00000256996.8:c.1013C>T	ENSP00000256996.3:p.Thr338Ile
ENST00000378600.7:c.457-2435C>T	ENSP00000367863.3:n.457-2435C>T
ENST00000378601.7:c.*100C>T	ENSP00000367864.3:n.*100C>T
ENST00000378603.7:c.821C>T	ENSP00000367866.3:p.Thr274Ile
ENST00000612309.4:n.2462C>T
ENST00000614394.1:n.403C>T
ENST00000616278.4:c.689C>T	ENSP00000478411.1:n.689C>T
ENST00000617022.4:n.1554-2435C>T
ENST00000617847.4:c.942C>T
ENST00000620515.1:n.179C>T
NM_000107.2:c.1013C>T , LRG_467t1:c.1013C>T	NP_000098.1:p.Thr338Ile
NM_001300734.1:c.457-2435C>T	NP_001287663.1:n.457-2435C>T
XR_242780.3:n.1003C>T
XR_242780.4:n.1003C>T
NM_000107.3:c.1013C>T MANE Select	NP_000098.1:p.Thr338Ile
NM_001300734.2:c.457-2435C>T	NP_001287663.1:n.457-2435C>T
NM_001399874.1:c.1013C>T	NP_001386803.1:p.Thr338Ile
NM_001399875.1:c.1013C>T	NP_001386804.1:p.Thr338Ile
NM_001399876.1:c.457-2435C>T	NP_001386805.1:n.457-2435C>T
NM_001399878.1:c.821C>T	NP_001386807.1:p.Thr274Ile
NR_174610.1:n.1264C>T
NR_174611.1:n.1242C>T