Canonical Allele Identifier: CA1969277878

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47215017G= , CM000673.2:g.47215017G=	GRCh38
NC_000011.9:g.47236568G= , CM000673.1:g.47236568G=	GRCh37
NC_000011.8:g.47193144G=	NCBI36
NG_009365.1:g.5076G= , LRG_467:g.5076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.-120G= MANE Select	ENSP00000256996.4:n.-120G=
ENST00000256996.8:c.-120G=	ENSP00000256996.3:n.-120G=
ENST00000378601.7:c.-120G=	ENSP00000367864.3:n.-120G=
ENST00000614825.4:c.-64-56G=	ENSP00000483718.1:n.-64-56G=
ENST00000622878.4:c.-66-54G=	ENSP00000479196.1:n.-66-54G=
NM_000107.2:c.-120G= , LRG_467t1:c.-120G=	NP_000098.1:n.-120G=
NM_001300734.1:c.-120G=	NP_001287663.1:n.-120G=
XR_242780.3:n.49G=
XR_242780.4:n.49G=
NM_000107.3:c.-120G= MANE Select	NP_000098.1:n.-120G=
NM_001300734.2:c.-120G=	NP_001287663.1:n.-120G=
NM_001399874.1:c.-66-54G=	NP_001386803.1:n.-66-54G=
NM_001399875.1:c.-64-56G=	NP_001386804.1:n.-64-56G=
NM_001399876.1:c.-66-54G=	NP_001386805.1:n.-66-54G=
NM_001399878.1:c.-120G=	NP_001386807.1:n.-120G=
NR_174610.1:n.222-54G=
NR_174611.1:n.222-54G=