Canonical Allele Identifier: CA1806681678

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224979G= , CM000670.2:g.102224979G=	GRCh38
NC_000008.10:g.103237207G= , CM000670.1:g.103237207G=	GRCh37
NC_000008.9:g.103306383G=	NCBI36
NG_016617.1:g.19140C= , LRG_788:g.19140C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.361C= MANE Select	ENSP00000251810.3:p.Arg121=
ENST00000251810.7:c.361C=	ENSP00000251810.3:p.Arg121=
ENST00000395912.6:c.205C=	ENSP00000379248.2:p.Arg69=
ENST00000519317.5:c.49-10821C=	ENSP00000430641.1:n.49-10821C=
ENST00000519962.5:c.48+13848C=	ENSP00000429140.1:n.48+13848C=
ENST00000522368.5:c.530C=
ENST00000522394.1:c.122+7252C=	ENSP00000429578.1:n.122+7252C=
ENST00000523957.1:c.*284C=	ENSP00000427830.1:n.*284C=
ENST00000621845.1:c.199C=	ENSP00000484318.1:p.Arg67=
NM_001172477.1:c.577C= , LRG_788t1:c.577C=	NP_001165948.1:p.Arg193=
NM_001172478.1:c.205C=	NP_001165949.1:p.Arg69=
NM_015713.4:c.361C= , LRG_788t2:c.361C=	NP_056528.2:p.Arg121=
NM_001172478.2:c.205C=	NP_001165949.1:p.Arg69=
NM_015713.5:c.361C= MANE Select	NP_056528.2:p.Arg121=