Canonical Allele Identifier: CA2613371061

Gene: DDB2

Linked Data

• gnomAD v4: 11-47216139-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47216139T>C , CM000673.2:g.47216139T>C	GRCh38
NC_000011.9:g.47237690T>C , CM000673.1:g.47237690T>C	GRCh37
NC_000011.8:g.47194266T>C	NCBI36
NG_009365.1:g.6198T>C , LRG_467:g.6198T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000256996.9:c.128-197T>C MANE Select	ENSP00000256996.4:n.128-197T>C
ENST00000256996.8:c.128-197T>C	ENSP00000256996.3:n.128-197T>C
ENST00000378600.7:c.128-197T>C	ENSP00000367863.3:n.128-197T>C
ENST00000378601.7:c.128-197T>C	ENSP00000367864.3:n.128-197T>C
ENST00000378603.7:c.128-197T>C	ENSP00000367866.3:n.128-197T>C
ENST00000610805.4:c.128-55T>C	ENSP00000478063.1:n.128-55T>C
ENST00000612309.4:n.1045T>C
ENST00000614825.4:c.128-197T>C	ENSP00000483718.1:n.128-197T>C
ENST00000615695.1:n.207-197T>C
ENST00000616278.4:c.128-197T>C	ENSP00000478411.1:n.128-197T>C
ENST00000617022.4:n.1028T>C
ENST00000622090.4:c.137-197T>C	ENSP00000479994.1:n.137-197T>C
ENST00000622878.4:c.128-197T>C	ENSP00000479196.1:n.128-197T>C
NM_000107.2:c.128-197T>C , LRG_467t1:c.128-197T>C	NP_000098.1:n.128-197T>C
NM_001300734.1:c.128-197T>C	NP_001287663.1:n.128-197T>C
XR_242780.3:n.296-197T>C
XR_242780.4:n.296-197T>C
NM_000107.3:c.128-197T>C MANE Select	NP_000098.1:n.128-197T>C
NM_001300734.2:c.128-197T>C	NP_001287663.1:n.128-197T>C
NM_001399874.1:c.128-197T>C	NP_001386803.1:n.128-197T>C
NM_001399875.1:c.128-197T>C	NP_001386804.1:n.128-197T>C
NM_001399876.1:c.128-197T>C	NP_001386805.1:n.128-197T>C
NM_001399878.1:c.128-197T>C	NP_001386807.1:n.128-197T>C
NR_174610.1:n.415-55T>C
NR_174611.1:n.415-197T>C