Canonical Allele Identifier: CA1806674666

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208160G= , CM000670.2:g.102208160G=	GRCh38
NC_000008.10:g.103220388G= , CM000670.1:g.103220388G=	GRCh37
NC_000008.9:g.103289564G=	NCBI36
NG_016617.1:g.35959C= , LRG_788:g.35959C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1029C= MANE Select	ENSP00000251810.3:p.Asn343=
ENST00000251810.7:c.1029C=	ENSP00000251810.3:p.Asn343=
ENST00000395910.6:n.416C=
ENST00000395912.6:c.873C=	ENSP00000379248.2:p.Asn291=
ENST00000519317.5:c.393C=	ENSP00000430641.1:p.Asn131=
ENST00000519962.5:c.174C=	ENSP00000429140.1:p.Asn58=
ENST00000522368.5:c.1198C=
ENST00000522394.1:c.362C=	ENSP00000429578.1:n.362C=
ENST00000621845.1:c.867C=	ENSP00000484318.1:p.Asn289=
NM_001172477.1:c.1245C= , LRG_788t1:c.1245C=	NP_001165948.1:p.Asn415=
NM_001172478.1:c.873C=	NP_001165949.1:p.Asn291=
NM_015713.4:c.1029C= , LRG_788t2:c.1029C=	NP_056528.2:p.Asn343=
NM_001172478.2:c.873C=	NP_001165949.1:p.Asn291=
NM_015713.5:c.1029C= MANE Select	NP_056528.2:p.Asn343=