Canonical Allele Identifier: CA380296929

Gene: DDB2

Linked Data

• gnomAD v4: 11-47235338-G-T
• MyVariant Identifiers: chr11:g.47256889G>T (hg19) ; chr11:g.47235338G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235338G>T , CM000673.2:g.47235338G>T	GRCh38
NC_000011.9:g.47256889G>T , CM000673.1:g.47256889G>T	GRCh37
NC_000011.8:g.47213465G>T	NCBI36
NG_009365.1:g.25397G>T , LRG_467:g.25397G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.949G>T MANE Select	ENSP00000256996.4:p.Ala317Ser
ENST00000256996.8:c.949G>T	ENSP00000256996.3:p.Ala317Ser
ENST00000378600.7:c.457-2499G>T	ENSP00000367863.3:n.457-2499G>T
ENST00000378601.7:c.*36G>T	ENSP00000367864.3:n.*36G>T
ENST00000378603.7:c.757G>T	ENSP00000367866.3:p.Ala253Ser
ENST00000612309.4:n.2398G>T
ENST00000614394.1:n.339G>T
ENST00000616278.4:c.625G>T	ENSP00000478411.1:n.625G>T
ENST00000617022.4:n.1554-2499G>T
ENST00000617847.4:c.878G>T
ENST00000620515.1:n.115G>T
NM_000107.2:c.949G>T , LRG_467t1:c.949G>T	NP_000098.1:p.Ala317Ser
NM_001300734.1:c.457-2499G>T	NP_001287663.1:n.457-2499G>T
XR_242780.3:n.939G>T
XR_242780.4:n.939G>T
NM_000107.3:c.949G>T MANE Select	NP_000098.1:p.Ala317Ser
NM_001300734.2:c.457-2499G>T	NP_001287663.1:n.457-2499G>T
NM_001399874.1:c.949G>T	NP_001386803.1:p.Ala317Ser
NM_001399875.1:c.949G>T	NP_001386804.1:p.Ala317Ser
NM_001399876.1:c.457-2499G>T	NP_001386805.1:n.457-2499G>T
NM_001399878.1:c.757G>T	NP_001386807.1:p.Ala253Ser
NR_174610.1:n.1200G>T
NR_174611.1:n.1178G>T