Canonical Allele Identifier: CA1806678358

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218918C= , CM000670.2:g.102218918C=	GRCh38
NC_000008.10:g.103231146C= , CM000670.1:g.103231146C=	GRCh37
NC_000008.9:g.103300322C=	NCBI36
NG_016617.1:g.25201G= , LRG_788:g.25201G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.580G= MANE Select	NP_056528.2:p.Glu194=
ENST00000251810.8:c.580G= MANE Select	ENSP00000251810.3:p.Glu194=
NM_001172477.1:c.796G= , LRG_788t1:c.796G=	NP_001165948.1:p.Glu266=
NM_001172478.1:c.424G=	NP_001165949.1:p.Glu142=
NM_001172478.2:c.424G=	NP_001165949.1:p.Glu142=
NM_015713.4:c.580G= , LRG_788t2:c.580G=	NP_056528.2:p.Glu194=
ENST00000251810.7:c.580G=	ENSP00000251810.3:p.Glu194=
ENST00000395912.6:c.424G=	ENSP00000379248.2:p.Glu142=
ENST00000519125.1:n.98G=
ENST00000519317.5:c.49-4760G=	ENSP00000430641.1:n.49-4760G=
ENST00000519962.5:c.49-10633G=	ENSP00000429140.1:n.49-10633G=
ENST00000522368.5:c.749G=
ENST00000522394.1:c.123-6029G=	ENSP00000429578.1:n.123-6029G=
ENST00000621845.1:c.418G=	ENSP00000484318.1:p.Glu140=