Canonical Allele Identifier: CA1806678234

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218846T= , CM000670.2:g.102218846T=	GRCh38
NC_000008.10:g.103231074T= , CM000670.1:g.103231074T=	GRCh37
NC_000008.9:g.103300250T=	NCBI36
NG_016617.1:g.25273A= , LRG_788:g.25273A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.652A= MANE Select	ENSP00000251810.3:p.Thr218=
ENST00000251810.7:c.652A=	ENSP00000251810.3:p.Thr218=
ENST00000395912.6:c.496A=	ENSP00000379248.2:p.Thr166=
ENST00000519125.1:n.170A=
ENST00000519317.5:c.49-4688A=	ENSP00000430641.1:n.49-4688A=
ENST00000519962.5:c.49-10561A=	ENSP00000429140.1:n.49-10561A=
ENST00000522368.5:c.821A=
ENST00000522394.1:c.123-5957A=	ENSP00000429578.1:n.123-5957A=
ENST00000621845.1:c.490A=	ENSP00000484318.1:p.Thr164=
NM_001172477.1:c.868A= , LRG_788t1:c.868A=	NP_001165948.1:p.Thr290=
NM_001172478.1:c.496A=	NP_001165949.1:p.Thr166=
NM_015713.4:c.652A= , LRG_788t2:c.652A=	NP_056528.2:p.Thr218=
NM_001172478.2:c.496A=	NP_001165949.1:p.Thr166=
NM_015713.5:c.652A= MANE Select	NP_056528.2:p.Thr218=