Canonical Allele Identifier: CA1806678406

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218942T= , CM000670.2:g.102218942T=	GRCh38
NC_000008.10:g.103231170T= , CM000670.1:g.103231170T=	GRCh37
NC_000008.9:g.103300346T=	NCBI36
NG_016617.1:g.25177A= , LRG_788:g.25177A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.556A= MANE Select	ENSP00000251810.3:p.Arg186=
ENST00000251810.7:c.556A=	ENSP00000251810.3:p.Arg186=
ENST00000395912.6:c.400A=	ENSP00000379248.2:p.Arg134=
ENST00000519125.1:n.74A=
ENST00000519317.5:c.49-4784A=	ENSP00000430641.1:n.49-4784A=
ENST00000519962.5:c.49-10657A=	ENSP00000429140.1:n.49-10657A=
ENST00000522368.5:c.725A=
ENST00000522394.1:c.123-6053A=	ENSP00000429578.1:n.123-6053A=
ENST00000621845.1:c.394A=	ENSP00000484318.1:p.Arg132=
NM_001172477.1:c.772A= , LRG_788t1:c.772A=	NP_001165948.1:p.Arg258=
NM_001172478.1:c.400A=	NP_001165949.1:p.Arg134=
NM_015713.4:c.556A= , LRG_788t2:c.556A=	NP_056528.2:p.Arg186=
NM_001172478.2:c.400A=	NP_001165949.1:p.Arg134=
NM_015713.5:c.556A= MANE Select	NP_056528.2:p.Arg186=