Canonical Allele Identifier: CA1806674667

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208167G= , CM000670.2:g.102208167G=	GRCh38
NC_000008.10:g.103220395G= , CM000670.1:g.103220395G=	GRCh37
NC_000008.9:g.103289571G=	NCBI36
NG_016617.1:g.35952C= , LRG_788:g.35952C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1022C= MANE Select	ENSP00000251810.3:p.Thr341=
ENST00000251810.7:c.1022C=	ENSP00000251810.3:p.Thr341=
ENST00000395910.6:n.409C=
ENST00000395912.6:c.866C=	ENSP00000379248.2:p.Thr289=
ENST00000519317.5:c.386C=	ENSP00000430641.1:p.Thr129=
ENST00000519962.5:c.167C=	ENSP00000429140.1:p.Thr56=
ENST00000522368.5:c.1191C=
ENST00000522394.1:c.355C=	ENSP00000429578.1:n.355C=
ENST00000621845.1:c.860C=	ENSP00000484318.1:p.Thr287=
NM_001172477.1:c.1238C= , LRG_788t1:c.1238C=	NP_001165948.1:p.Thr413=
NM_001172478.1:c.866C=	NP_001165949.1:p.Thr289=
NM_015713.4:c.1022C= , LRG_788t2:c.1022C=	NP_056528.2:p.Thr341=
NM_001172478.2:c.866C=	NP_001165949.1:p.Thr289=
NM_015713.5:c.1022C= MANE Select	NP_056528.2:p.Thr341=