Canonical Allele Identifier: CA1806681668

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224949C= , CM000670.2:g.102224949C=	GRCh38
NC_000008.10:g.103237177C= , CM000670.1:g.103237177C=	GRCh37
NC_000008.9:g.103306353C=	NCBI36
NG_016617.1:g.19170G= , LRG_788:g.19170G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.391G= MANE Select	NP_056528.2:p.Glu131=
ENST00000251810.8:c.391G= MANE Select	ENSP00000251810.3:p.Glu131=
NM_001172477.1:c.607G= , LRG_788t1:c.607G=	NP_001165948.1:p.Glu203=
NM_001172478.1:c.235G=	NP_001165949.1:p.Glu79=
NM_001172478.2:c.235G=	NP_001165949.1:p.Glu79=
NM_015713.4:c.391G= , LRG_788t2:c.391G=	NP_056528.2:p.Glu131=
ENST00000251810.7:c.391G=	ENSP00000251810.3:p.Glu131=
ENST00000395912.6:c.235G=	ENSP00000379248.2:p.Glu79=
ENST00000519317.5:c.49-10791G=	ENSP00000430641.1:n.49-10791G=
ENST00000519962.5:c.48+13878G=	ENSP00000429140.1:n.48+13878G=
ENST00000522368.5:c.560G=
ENST00000522394.1:c.122+7282G=	ENSP00000429578.1:n.122+7282G=
ENST00000523957.1:c.*314G=	ENSP00000427830.1:n.*314G=
ENST00000621845.1:c.229G=	ENSP00000484318.1:p.Glu77=