Canonical Allele Identifier: CA380296738

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256853A>T (hg19) ; chr11:g.47235302A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235302A>T , CM000673.2:g.47235302A>T	GRCh38
NC_000011.9:g.47256853A>T , CM000673.1:g.47256853A>T	GRCh37
NC_000011.8:g.47213429A>T	NCBI36
NG_009365.1:g.25361A>T , LRG_467:g.25361A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.913A>T MANE Select	ENSP00000256996.4:p.Thr305Ser
ENST00000256996.8:c.913A>T	ENSP00000256996.3:p.Thr305Ser
ENST00000378600.7:c.457-2535A>T	ENSP00000367863.3:n.457-2535A>T
ENST00000378601.7:c.735A>T	ENSP00000367864.3:p.Ter245Cys
ENST00000378603.7:c.721A>T	ENSP00000367866.3:p.Thr241Ser
ENST00000612309.4:n.2362A>T
ENST00000614394.1:n.303A>T
ENST00000616278.4:c.589A>T	ENSP00000478411.1:n.589A>T
ENST00000617022.4:n.1554-2535A>T
ENST00000617847.4:c.842A>T
ENST00000620515.1:n.79A>T
NM_000107.2:c.913A>T , LRG_467t1:c.913A>T	NP_000098.1:p.Thr305Ser
NM_001300734.1:c.457-2535A>T	NP_001287663.1:n.457-2535A>T
XR_242780.3:n.903A>T
XR_242780.4:n.903A>T
NM_000107.3:c.913A>T MANE Select	NP_000098.1:p.Thr305Ser
NM_001300734.2:c.457-2535A>T	NP_001287663.1:n.457-2535A>T
NM_001399874.1:c.913A>T	NP_001386803.1:p.Thr305Ser
NM_001399875.1:c.913A>T	NP_001386804.1:p.Thr305Ser
NM_001399876.1:c.457-2535A>T	NP_001386805.1:n.457-2535A>T
NM_001399878.1:c.721A>T	NP_001386807.1:p.Thr241Ser
NR_174610.1:n.1164A>T
NR_174611.1:n.1142A>T