Canonical Allele Identifier: CA1806681646

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224882T= , CM000670.2:g.102224882T=	GRCh38
NC_000008.10:g.103237110T= , CM000670.1:g.103237110T=	GRCh37
NC_000008.9:g.103306286T=	NCBI36
NG_016617.1:g.19237A= , LRG_788:g.19237A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.455+3A= MANE Select	ENSP00000251810.3:n.455+3A=
ENST00000251810.7:c.455+3A=	ENSP00000251810.3:n.455+3A=
ENST00000395912.6:c.299+3A=	ENSP00000379248.2:n.299+3A=
ENST00000519317.5:c.49-10724A=	ENSP00000430641.1:n.49-10724A=
ENST00000519962.5:c.48+13945A=	ENSP00000429140.1:n.48+13945A=
ENST00000522368.5:c.624+3A=
ENST00000522394.1:c.122+7349A=	ENSP00000429578.1:n.122+7349A=
ENST00000621845.1:c.293+3A=	ENSP00000484318.1:n.293+3A=
NM_001172477.1:c.671+3A= , LRG_788t1:c.671+3A=	NP_001165948.1:n.671+3A=
NM_001172478.1:c.299+3A=	NP_001165949.1:n.299+3A=
NM_015713.4:c.455+3A= , LRG_788t2:c.455+3A=	NP_056528.2:n.455+3A=
NM_001172478.2:c.299+3A=	NP_001165949.1:n.299+3A=
NM_015713.5:c.455+3A= MANE Select	NP_056528.2:n.455+3A=