Canonical Allele Identifier: CA221687313

Gene: DDB2

Linked Data

• dbSNP Id: rs77026843
• gnomAD v4: 11-47235079-T-G
• MyVariant Identifiers: chr11:g.47256630T>G (hg19) ; chr11:g.47235079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235079T>G , CM000673.2:g.47235079T>G	GRCh38
NC_000011.9:g.47256630T>G , CM000673.1:g.47256630T>G	GRCh37
NC_000011.8:g.47213206T>G	NCBI36
NG_009365.1:g.25138T>G , LRG_467:g.25138T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+145T>G MANE Select	ENSP00000256996.4:n.880+145T>G
ENST00000256996.8:c.880+145T>G	ENSP00000256996.3:n.880+145T>G
ENST00000378600.7:c.457-2758T>G	ENSP00000367863.3:n.457-2758T>G
ENST00000378601.7:c.703-191T>G	ENSP00000367864.3:n.703-191T>G
ENST00000378603.7:c.688+145T>G	ENSP00000367866.3:n.688+145T>G
ENST00000612309.4:n.2139T>G
ENST00000614394.1:n.270+145T>G
ENST00000616278.4:c.557-191T>G	ENSP00000478411.1:n.557-191T>G
ENST00000617022.4:n.1554-2758T>G
ENST00000617847.4:c.809+145T>G
ENST00000620515.1:n.47-191T>G
NM_000107.2:c.880+145T>G , LRG_467t1:c.880+145T>G	NP_000098.1:n.880+145T>G
NM_001300734.1:c.457-2758T>G	NP_001287663.1:n.457-2758T>G
XR_242780.3:n.871-191T>G
XR_242780.4:n.871-191T>G
NM_000107.3:c.880+145T>G MANE Select	NP_000098.1:n.880+145T>G
NM_001300734.2:c.457-2758T>G	NP_001287663.1:n.457-2758T>G
NM_001399874.1:c.880+145T>G	NP_001386803.1:n.880+145T>G
NM_001399875.1:c.880+145T>G	NP_001386804.1:n.880+145T>G
NM_001399876.1:c.457-2758T>G	NP_001386805.1:n.457-2758T>G
NM_001399878.1:c.688+145T>G	NP_001386807.1:n.688+145T>G
NR_174610.1:n.1132-191T>G
NR_174611.1:n.1110-191T>G