Canonical Allele Identifier: CA1969296882

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235171G= , CM000673.2:g.47235171G=	GRCh38
NC_000011.9:g.47256722G= , CM000673.1:g.47256722G=	GRCh37
NC_000011.8:g.47213298G=	NCBI36
NG_009365.1:g.25230G= , LRG_467:g.25230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.881-99G= MANE Select	ENSP00000256996.4:n.881-99G=
ENST00000256996.8:c.881-99G=	ENSP00000256996.3:n.881-99G=
ENST00000378600.7:c.457-2666G=	ENSP00000367863.3:n.457-2666G=
ENST00000378601.7:c.703-99G=	ENSP00000367864.3:n.703-99G=
ENST00000378603.7:c.689-99G=	ENSP00000367866.3:n.689-99G=
ENST00000612309.4:n.2231G=
ENST00000614394.1:n.271-99G=
ENST00000616278.4:c.557-99G=	ENSP00000478411.1:n.557-99G=
ENST00000617022.4:n.1554-2666G=
ENST00000617847.4:c.810-99G=
ENST00000620515.1:n.47-99G=
NM_000107.2:c.881-99G= , LRG_467t1:c.881-99G=	NP_000098.1:n.881-99G=
NM_001300734.1:c.457-2666G=	NP_001287663.1:n.457-2666G=
XR_242780.3:n.871-99G=
XR_242780.4:n.871-99G=
NM_000107.3:c.881-99G= MANE Select	NP_000098.1:n.881-99G=
NM_001300734.2:c.457-2666G=	NP_001287663.1:n.457-2666G=
NM_001399874.1:c.881-99G=	NP_001386803.1:n.881-99G=
NM_001399875.1:c.881-99G=	NP_001386804.1:n.881-99G=
NM_001399876.1:c.457-2666G=	NP_001386805.1:n.457-2666G=
NM_001399878.1:c.689-99G=	NP_001386807.1:n.689-99G=
NR_174610.1:n.1132-99G=
NR_174611.1:n.1110-99G=