Canonical Allele Identifier: CA3156357485

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218863C= , CM000670.2:g.102218863C=	GRCh38
NC_000008.10:g.103231091C= , CM000670.1:g.103231091C=	GRCh37
NC_000008.9:g.103300267C=	NCBI36
NG_016617.1:g.25256G= , LRG_788:g.25256G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.635G= MANE Select	ENSP00000251810.3:p.Gly212=
ENST00000251810.7:c.635G=	ENSP00000251810.3:p.Gly212=
ENST00000395912.6:c.479G=	ENSP00000379248.2:p.Gly160=
ENST00000519125.1:n.153G=
ENST00000519317.5:c.49-4705G=	ENSP00000430641.1:n.49-4705G=
ENST00000519962.5:c.49-10578G=	ENSP00000429140.1:n.49-10578G=
ENST00000522368.5:c.804G=
ENST00000522394.1:c.123-5974G=	ENSP00000429578.1:n.123-5974G=
ENST00000621845.1:c.473G=	ENSP00000484318.1:p.Gly158=
NM_001172477.1:c.851G= , LRG_788t1:c.851G=	NP_001165948.1:p.Gly284=
NM_001172478.1:c.479G=	NP_001165949.1:p.Gly160=
NM_015713.4:c.635G= , LRG_788t2:c.635G=	NP_056528.2:p.Gly212=
NM_001172478.2:c.479G=	NP_001165949.1:p.Gly160=
NM_015713.5:c.635G= MANE Select	NP_056528.2:p.Gly212=