Canonical Allele Identifier: CA1806686196

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232153T= , CM000670.2:g.102232153T=	GRCh38
NC_000008.10:g.103244381T= , CM000670.1:g.103244381T=	GRCh37
NC_000008.9:g.103313557T=	NCBI36
NG_016617.1:g.11966A= , LRG_788:g.11966A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.200A= MANE Select	ENSP00000251810.3:p.Glu67=
ENST00000251810.7:c.200A=	ENSP00000251810.3:p.Glu67=
ENST00000395912.6:c.49-6119A=	ENSP00000379248.2:n.49-6119A=
ENST00000517517.1:n.509A=
ENST00000519317.5:c.48+6674A=	ENSP00000430641.1:n.48+6674A=
ENST00000519962.5:c.48+6674A=	ENSP00000429140.1:n.48+6674A=
ENST00000522368.5:c.369A=
ENST00000522394.1:c.122+78A=	ENSP00000429578.1:n.122+78A=
ENST00000523957.1:c.*123A=	ENSP00000427830.1:n.*123A=
ENST00000621845.1:c.38A=	ENSP00000484318.1:p.Glu13=
NM_001172477.1:c.416A= , LRG_788t1:c.416A=	NP_001165948.1:p.Glu139=
NM_001172478.1:c.49-6119A=	NP_001165949.1:n.49-6119A=
NM_015713.4:c.200A= , LRG_788t2:c.200A=	NP_056528.2:p.Glu67=
NM_001172478.2:c.49-6119A=	NP_001165949.1:n.49-6119A=
NM_015713.5:c.200A= MANE Select	NP_056528.2:p.Glu67=