Canonical Allele Identifier: CA1806674678

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208210G= , CM000670.2:g.102208210G=	GRCh38
NC_000008.10:g.103220438G= , CM000670.1:g.103220438G=	GRCh37
NC_000008.9:g.103289614G=	NCBI36
NG_016617.1:g.35909C= , LRG_788:g.35909C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.979C= MANE Select	ENSP00000251810.3:p.Arg327=
ENST00000251810.7:c.979C=	ENSP00000251810.3:p.Arg327=
ENST00000395910.6:n.366C=
ENST00000395912.6:c.823C=	ENSP00000379248.2:p.Arg275=
ENST00000519317.5:c.343C=	ENSP00000430641.1:p.Arg115=
ENST00000519962.5:c.124C=	ENSP00000429140.1:p.Arg42=
ENST00000522368.5:c.1148C=
ENST00000522394.1:c.312C=	ENSP00000429578.1:n.312C=
ENST00000621845.1:c.817C=	ENSP00000484318.1:p.Arg273=
NM_001172477.1:c.1195C= , LRG_788t1:c.1195C=	NP_001165948.1:p.Arg399=
NM_001172478.1:c.823C=	NP_001165949.1:p.Arg275=
NM_015713.4:c.979C= , LRG_788t2:c.979C=	NP_056528.2:p.Arg327=
NM_001172478.2:c.823C=	NP_001165949.1:p.Arg275=
NM_015713.5:c.979C= MANE Select	NP_056528.2:p.Arg327=