Canonical Allele Identifier: CA1806674685

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208237C= , CM000670.2:g.102208237C=	GRCh38
NC_000008.10:g.103220465C= , CM000670.1:g.103220465C=	GRCh37
NC_000008.9:g.103289641C=	NCBI36
NG_016617.1:g.35882G= , LRG_788:g.35882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.952G= MANE Select	ENSP00000251810.3:p.Glu318=
ENST00000251810.7:c.952G=	ENSP00000251810.3:p.Glu318=
ENST00000395910.6:n.339G=
ENST00000395912.6:c.796G=	ENSP00000379248.2:p.Glu266=
ENST00000519317.5:c.316G=	ENSP00000430641.1:p.Glu106=
ENST00000519962.5:c.97G=	ENSP00000429140.1:p.Glu33=
ENST00000522368.5:c.1121G=
ENST00000522394.1:c.285G=	ENSP00000429578.1:n.285G=
ENST00000621845.1:c.790G=	ENSP00000484318.1:p.Glu264=
NM_001172477.1:c.1168G= , LRG_788t1:c.1168G=	NP_001165948.1:p.Glu390=
NM_001172478.1:c.796G=	NP_001165949.1:p.Glu266=
NM_015713.4:c.952G= , LRG_788t2:c.952G=	NP_056528.2:p.Glu318=
NM_001172478.2:c.796G=	NP_001165949.1:p.Glu266=
NM_015713.5:c.952G= MANE Select	NP_056528.2:p.Glu318=