Canonical Allele Identifier: CA1806674663

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208154G= , CM000670.2:g.102208154G=	GRCh38
NC_000008.10:g.103220382G= , CM000670.1:g.103220382G=	GRCh37
NC_000008.9:g.103289558G=	NCBI36
NG_016617.1:g.35965C= , LRG_788:g.35965C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1035C= MANE Select	ENSP00000251810.3:p.Phe345=
ENST00000251810.7:c.1035C=	ENSP00000251810.3:p.Phe345=
ENST00000395910.6:n.422C=
ENST00000395912.6:c.879C=	ENSP00000379248.2:p.Phe293=
ENST00000519317.5:c.399C=	ENSP00000430641.1:p.Phe133=
ENST00000519962.5:c.180C=	ENSP00000429140.1:p.Phe60=
ENST00000522368.5:c.1204C=
ENST00000522394.1:c.368C=	ENSP00000429578.1:n.368C=
ENST00000621845.1:c.873C=	ENSP00000484318.1:p.Phe291=
NM_001172477.1:c.1251C= , LRG_788t1:c.1251C=	NP_001165948.1:p.Phe417=
NM_001172478.1:c.879C=	NP_001165949.1:p.Phe293=
NM_015713.4:c.1035C= , LRG_788t2:c.1035C=	NP_056528.2:p.Phe345=
NM_001172478.2:c.879C=	NP_001165949.1:p.Phe293=
NM_015713.5:c.1035C= MANE Select	NP_056528.2:p.Phe345=