Canonical Allele Identifier: CA380297170

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256938A>C (hg19) ; chr11:g.47235387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235387A>C , CM000673.2:g.47235387A>C	GRCh38
NC_000011.9:g.47256938A>C , CM000673.1:g.47256938A>C	GRCh37
NC_000011.8:g.47213514A>C	NCBI36
NG_009365.1:g.25446A>C , LRG_467:g.25446A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.998A>C MANE Select	ENSP00000256996.4:p.His333Pro
ENST00000256996.8:c.998A>C	ENSP00000256996.3:p.His333Pro
ENST00000378600.7:c.457-2450A>C	ENSP00000367863.3:n.457-2450A>C
ENST00000378601.7:c.*85A>C	ENSP00000367864.3:n.*85A>C
ENST00000378603.7:c.806A>C	ENSP00000367866.3:p.His269Pro
ENST00000612309.4:n.2447A>C
ENST00000614394.1:n.388A>C
ENST00000616278.4:c.674A>C	ENSP00000478411.1:n.674A>C
ENST00000617022.4:n.1554-2450A>C
ENST00000617847.4:c.927A>C
ENST00000620515.1:n.164A>C
NM_000107.2:c.998A>C , LRG_467t1:c.998A>C	NP_000098.1:p.His333Pro
NM_001300734.1:c.457-2450A>C	NP_001287663.1:n.457-2450A>C
XR_242780.3:n.988A>C
XR_242780.4:n.988A>C
NM_000107.3:c.998A>C MANE Select	NP_000098.1:p.His333Pro
NM_001300734.2:c.457-2450A>C	NP_001287663.1:n.457-2450A>C
NM_001399874.1:c.998A>C	NP_001386803.1:p.His333Pro
NM_001399875.1:c.998A>C	NP_001386804.1:p.His333Pro
NM_001399876.1:c.457-2450A>C	NP_001386805.1:n.457-2450A>C
NM_001399878.1:c.806A>C	NP_001386807.1:p.His269Pro
NR_174610.1:n.1249A>C
NR_174611.1:n.1227A>C