Canonical Allele Identifier: CA1806674665

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208159C= , CM000670.2:g.102208159C=	GRCh38
NC_000008.10:g.103220387C= , CM000670.1:g.103220387C=	GRCh37
NC_000008.9:g.103289563C=	NCBI36
NG_016617.1:g.35960G= , LRG_788:g.35960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1030G= MANE Select	ENSP00000251810.3:p.Val344=
ENST00000251810.7:c.1030G=	ENSP00000251810.3:p.Val344=
ENST00000395910.6:n.417G=
ENST00000395912.6:c.874G=	ENSP00000379248.2:p.Val292=
ENST00000519317.5:c.394G=	ENSP00000430641.1:p.Val132=
ENST00000519962.5:c.175G=	ENSP00000429140.1:p.Val59=
ENST00000522368.5:c.1199G=
ENST00000522394.1:c.363G=	ENSP00000429578.1:n.363G=
ENST00000621845.1:c.868G=	ENSP00000484318.1:p.Val290=
NM_001172477.1:c.1246G= , LRG_788t1:c.1246G=	NP_001165948.1:p.Val416=
NM_001172478.1:c.874G=	NP_001165949.1:p.Val292=
NM_015713.4:c.1030G= , LRG_788t2:c.1030G=	NP_056528.2:p.Val344=
NM_001172478.2:c.874G=	NP_001165949.1:p.Val292=
NM_015713.5:c.1030G= MANE Select	NP_056528.2:p.Val344=