Canonical Allele Identifier: CA1806681676

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224972A= , CM000670.2:g.102224972A=	GRCh38
NC_000008.10:g.103237200A= , CM000670.1:g.103237200A=	GRCh37
NC_000008.9:g.103306376A=	NCBI36
NG_016617.1:g.19147T= , LRG_788:g.19147T=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.368T= MANE Select	NP_056528.2:p.Phe123=
ENST00000251810.8:c.368T= MANE Select	ENSP00000251810.3:p.Phe123=
NM_001172477.1:c.584T= , LRG_788t1:c.584T=	NP_001165948.1:p.Phe195=
NM_001172478.1:c.212T=	NP_001165949.1:p.Phe71=
NM_001172478.2:c.212T=	NP_001165949.1:p.Phe71=
NM_015713.4:c.368T= , LRG_788t2:c.368T=	NP_056528.2:p.Phe123=
ENST00000251810.7:c.368T=	ENSP00000251810.3:p.Phe123=
ENST00000395912.6:c.212T=	ENSP00000379248.2:p.Phe71=
ENST00000519317.5:c.49-10814T=	ENSP00000430641.1:n.49-10814T=
ENST00000519962.5:c.48+13855T=	ENSP00000429140.1:n.48+13855T=
ENST00000522368.5:c.537T=
ENST00000522394.1:c.122+7259T=	ENSP00000429578.1:n.122+7259T=
ENST00000523957.1:c.*291T=	ENSP00000427830.1:n.*291T=
ENST00000621845.1:c.206T=	ENSP00000484318.1:p.Phe69=