Canonical Allele Identifier: CA1806686195

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232150T= , CM000670.2:g.102232150T=	GRCh38
NC_000008.10:g.103244378T= , CM000670.1:g.103244378T=	GRCh37
NC_000008.9:g.103313554T=	NCBI36
NG_016617.1:g.11969A= , LRG_788:g.11969A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.203A= MANE Select	ENSP00000251810.3:p.Glu68=
ENST00000251810.7:c.203A=	ENSP00000251810.3:p.Glu68=
ENST00000395912.6:c.49-6116A=	ENSP00000379248.2:n.49-6116A=
ENST00000517517.1:n.512A=
ENST00000519317.5:c.48+6677A=	ENSP00000430641.1:n.48+6677A=
ENST00000519962.5:c.48+6677A=	ENSP00000429140.1:n.48+6677A=
ENST00000522368.5:c.372A=
ENST00000522394.1:c.122+81A=	ENSP00000429578.1:n.122+81A=
ENST00000523957.1:c.*126A=	ENSP00000427830.1:n.*126A=
ENST00000621845.1:c.41A=	ENSP00000484318.1:p.Glu14=
NM_001172477.1:c.419A= , LRG_788t1:c.419A=	NP_001165948.1:p.Glu140=
NM_001172478.1:c.49-6116A=	NP_001165949.1:n.49-6116A=
NM_015713.4:c.203A= , LRG_788t2:c.203A=	NP_056528.2:p.Glu68=
NM_001172478.2:c.49-6116A=	NP_001165949.1:n.49-6116A=
NM_015713.5:c.203A= MANE Select	NP_056528.2:p.Glu68=