Canonical Allele Identifier: CA1806686202

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232177G= , CM000670.2:g.102232177G=	GRCh38
NC_000008.10:g.103244405G= , CM000670.1:g.103244405G=	GRCh37
NC_000008.9:g.103313581G=	NCBI36
NG_016617.1:g.11942C= , LRG_788:g.11942C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.176C= MANE Select	ENSP00000251810.3:p.Ala59=
ENST00000251810.7:c.176C=	ENSP00000251810.3:p.Ala59=
ENST00000395912.6:c.49-6143C=	ENSP00000379248.2:n.49-6143C=
ENST00000517517.1:n.485C=
ENST00000519317.5:c.48+6650C=	ENSP00000430641.1:n.48+6650C=
ENST00000519962.5:c.48+6650C=	ENSP00000429140.1:n.48+6650C=
ENST00000522368.5:c.345C=
ENST00000522394.1:c.122+54C=	ENSP00000429578.1:n.122+54C=
ENST00000523957.1:c.*99C=	ENSP00000427830.1:n.*99C=
ENST00000621845.1:c.14C=	ENSP00000484318.1:p.Ala5=
NM_001172477.1:c.392C= , LRG_788t1:c.392C=	NP_001165948.1:p.Ala131=
NM_001172478.1:c.49-6143C=	NP_001165949.1:n.49-6143C=
NM_015713.4:c.176C= , LRG_788t2:c.176C=	NP_056528.2:p.Ala59=
NM_001172478.2:c.49-6143C=	NP_001165949.1:n.49-6143C=
NM_015713.5:c.176C= MANE Select	NP_056528.2:p.Ala59=