Canonical Allele Identifier: CA380296766

Gene: DDB2

Linked Data

• dbSNP Id: rs121434642
• gnomAD v4: 11-47235308-G-A
• MyVariant Identifiers: chr11:g.47256859G>A (hg19) ; chr11:g.47235308G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235308G>A , CM000673.2:g.47235308G>A	GRCh38
NC_000011.9:g.47256859G>A , CM000673.1:g.47256859G>A	GRCh37
NC_000011.8:g.47213435G>A	NCBI36
NG_009365.1:g.25367G>A , LRG_467:g.25367G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000256996.9:c.919G>A MANE Select	ENSP00000256996.4:p.Asp307Asn
ENST00000256996.8:c.919G>A	ENSP00000256996.3:p.Asp307Asn
ENST00000378600.7:c.457-2529G>A	ENSP00000367863.3:n.457-2529G>A
ENST00000378601.7:c.*6G>A	ENSP00000367864.3:n.*6G>A
ENST00000378603.7:c.727G>A	ENSP00000367866.3:p.Asp243Asn
ENST00000612309.4:n.2368G>A
ENST00000614394.1:n.309G>A
ENST00000616278.4:c.595G>A	ENSP00000478411.1:n.595G>A
ENST00000617022.4:n.1554-2529G>A
ENST00000617847.4:c.848G>A
ENST00000620515.1:n.85G>A
NM_000107.2:c.919G>A , LRG_467t1:c.919G>A	NP_000098.1:p.Asp307Asn
NM_001300734.1:c.457-2529G>A	NP_001287663.1:n.457-2529G>A
XR_242780.3:n.909G>A
XR_242780.4:n.909G>A
NM_000107.3:c.919G>A MANE Select	NP_000098.1:p.Asp307Asn
NM_001300734.2:c.457-2529G>A	NP_001287663.1:n.457-2529G>A
NM_001399874.1:c.919G>A	NP_001386803.1:p.Asp307Asn
NM_001399875.1:c.919G>A	NP_001386804.1:p.Asp307Asn
NM_001399876.1:c.457-2529G>A	NP_001386805.1:n.457-2529G>A
NM_001399878.1:c.727G>A	NP_001386807.1:p.Asp243Asn
NR_174610.1:n.1170G>A
NR_174611.1:n.1148G>A