Canonical Allele Identifier: CA1806681679

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224981G= , CM000670.2:g.102224981G=	GRCh38
NC_000008.10:g.103237209G= , CM000670.1:g.103237209G=	GRCh37
NC_000008.9:g.103306385G=	NCBI36
NG_016617.1:g.19138C= , LRG_788:g.19138C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.359C= MANE Select	ENSP00000251810.3:p.Ala120=
ENST00000251810.7:c.359C=	ENSP00000251810.3:p.Ala120=
ENST00000395912.6:c.203C=	ENSP00000379248.2:p.Ala68=
ENST00000519317.5:c.49-10823C=	ENSP00000430641.1:n.49-10823C=
ENST00000519962.5:c.48+13846C=	ENSP00000429140.1:n.48+13846C=
ENST00000522368.5:c.528C=
ENST00000522394.1:c.122+7250C=	ENSP00000429578.1:n.122+7250C=
ENST00000523957.1:c.*282C=	ENSP00000427830.1:n.*282C=
ENST00000621845.1:c.197C=	ENSP00000484318.1:p.Ala66=
NM_001172477.1:c.575C= , LRG_788t1:c.575C=	NP_001165948.1:p.Ala192=
NM_001172478.1:c.203C=	NP_001165949.1:p.Ala68=
NM_015713.4:c.359C= , LRG_788t2:c.359C=	NP_056528.2:p.Ala120=
NM_001172478.2:c.203C=	NP_001165949.1:p.Ala68=
NM_015713.5:c.359C= MANE Select	NP_056528.2:p.Ala120=