Canonical Allele Identifier: CA1806674664

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208158A= , CM000670.2:g.102208158A=	GRCh38
NC_000008.10:g.103220386A= , CM000670.1:g.103220386A=	GRCh37
NC_000008.9:g.103289562A=	NCBI36
NG_016617.1:g.35961T= , LRG_788:g.35961T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1031T= MANE Select	ENSP00000251810.3:p.Val344=
ENST00000251810.7:c.1031T=	ENSP00000251810.3:p.Val344=
ENST00000395910.6:n.418T=
ENST00000395912.6:c.875T=	ENSP00000379248.2:p.Val292=
ENST00000519317.5:c.395T=	ENSP00000430641.1:p.Val132=
ENST00000519962.5:c.176T=	ENSP00000429140.1:p.Val59=
ENST00000522368.5:c.1200T=
ENST00000522394.1:c.364T=	ENSP00000429578.1:n.364T=
ENST00000621845.1:c.869T=	ENSP00000484318.1:p.Val290=
NM_001172477.1:c.1247T= , LRG_788t1:c.1247T=	NP_001165948.1:p.Val416=
NM_001172478.1:c.875T=	NP_001165949.1:p.Val292=
NM_015713.4:c.1031T= , LRG_788t2:c.1031T=	NP_056528.2:p.Val344=
NM_001172478.2:c.875T=	NP_001165949.1:p.Val292=
NM_015713.5:c.1031T= MANE Select	NP_056528.2:p.Val344=