Canonical Allele Identifier: CA1806678303

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218892A= , CM000670.2:g.102218892A=	GRCh38
NC_000008.10:g.103231120A= , CM000670.1:g.103231120A=	GRCh37
NC_000008.9:g.103300296A=	NCBI36
NG_016617.1:g.25227T= , LRG_788:g.25227T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.606T= MANE Select	ENSP00000251810.3:p.Phe202=
ENST00000251810.7:c.606T=	ENSP00000251810.3:p.Phe202=
ENST00000395912.6:c.450T=	ENSP00000379248.2:p.Phe150=
ENST00000519125.1:n.124T=
ENST00000519317.5:c.49-4734T=	ENSP00000430641.1:n.49-4734T=
ENST00000519962.5:c.49-10607T=	ENSP00000429140.1:n.49-10607T=
ENST00000522368.5:c.775T=
ENST00000522394.1:c.123-6003T=	ENSP00000429578.1:n.123-6003T=
ENST00000621845.1:c.444T=	ENSP00000484318.1:p.Phe148=
NM_001172477.1:c.822T= , LRG_788t1:c.822T=	NP_001165948.1:p.Phe274=
NM_001172478.1:c.450T=	NP_001165949.1:p.Phe150=
NM_015713.4:c.606T= , LRG_788t2:c.606T=	NP_056528.2:p.Phe202=
NM_001172478.2:c.450T=	NP_001165949.1:p.Phe150=
NM_015713.5:c.606T= MANE Select	NP_056528.2:p.Phe202=