Canonical Allele Identifier: CA1806681278

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224076G= , CM000670.2:g.102224076G=	GRCh38
NC_000008.10:g.103236304G= , CM000670.1:g.103236304G=	GRCh37
NC_000008.9:g.103305480G=	NCBI36
NG_016617.1:g.20043C= , LRG_788:g.20043C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.520C= MANE Select	NP_056528.2:p.Arg174=
ENST00000251810.8:c.520C= MANE Select	ENSP00000251810.3:p.Arg174=
NM_001172477.1:c.736C= , LRG_788t1:c.736C=	NP_001165948.1:p.Arg246=
NM_001172478.1:c.364C=	NP_001165949.1:p.Arg122=
NM_001172478.2:c.364C=	NP_001165949.1:p.Arg122=
NM_015713.4:c.520C= , LRG_788t2:c.520C=	NP_056528.2:p.Arg174=
ENST00000251810.7:c.520C=	ENSP00000251810.3:p.Arg174=
ENST00000395912.6:c.364C=	ENSP00000379248.2:p.Arg122=
ENST00000519317.5:c.49-9918C=	ENSP00000430641.1:n.49-9918C=
ENST00000519962.5:c.48+14751C=	ENSP00000429140.1:n.48+14751C=
ENST00000522368.5:c.689C=
ENST00000522394.1:c.122+8155C=	ENSP00000429578.1:n.122+8155C=
ENST00000621845.1:c.358C=	ENSP00000484318.1:p.Arg120=