Canonical Allele Identifier: CA1806677103

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102214136C= , CM000670.2:g.102214136C=	GRCh38
NC_000008.10:g.103226364C= , CM000670.1:g.103226364C=	GRCh37
NC_000008.9:g.103295540C=	NCBI36
NG_016617.1:g.29983G= , LRG_788:g.29983G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.707G= MANE Select	ENSP00000251810.3:p.Cys236=
ENST00000251810.7:c.707G=	ENSP00000251810.3:p.Cys236=
ENST00000395910.6:n.94G=
ENST00000395912.6:c.551G=	ENSP00000379248.2:p.Cys184=
ENST00000519125.1:n.225G=
ENST00000519317.5:c.71G=	ENSP00000430641.1:p.Cys24=
ENST00000519962.5:c.49-5851G=	ENSP00000429140.1:n.49-5851G=
ENST00000522368.5:c.876G=
ENST00000522394.1:c.123-1247G=	ENSP00000429578.1:n.123-1247G=
ENST00000621845.1:c.545G=	ENSP00000484318.1:p.Cys182=
NM_001172477.1:c.923G= , LRG_788t1:c.923G=	NP_001165948.1:p.Cys308=
NM_001172478.1:c.551G=	NP_001165949.1:p.Cys184=
NM_015713.4:c.707G= , LRG_788t2:c.707G=	NP_056528.2:p.Cys236=
NM_001172478.2:c.551G=	NP_001165949.1:p.Cys184=
NM_015713.5:c.707G= MANE Select	NP_056528.2:p.Cys236=