Canonical Allele Identifier: CA1806678225

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218836T= , CM000670.2:g.102218836T=	GRCh38
NC_000008.10:g.103231064T= , CM000670.1:g.103231064T=	GRCh37
NC_000008.9:g.103300240T=	NCBI36
NG_016617.1:g.25283A= , LRG_788:g.25283A=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.662A= MANE Select	NP_056528.2:p.Asn221=
ENST00000251810.8:c.662A= MANE Select	ENSP00000251810.3:p.Asn221=
NM_001172477.1:c.878A= , LRG_788t1:c.878A=	NP_001165948.1:p.Asn293=
NM_001172478.1:c.506A=	NP_001165949.1:p.Asn169=
NM_001172478.2:c.506A=	NP_001165949.1:p.Asn169=
NM_015713.4:c.662A= , LRG_788t2:c.662A=	NP_056528.2:p.Asn221=
ENST00000251810.7:c.662A=	ENSP00000251810.3:p.Asn221=
ENST00000395912.6:c.506A=	ENSP00000379248.2:p.Asn169=
ENST00000519125.1:n.180A=
ENST00000519317.5:c.49-4678A=	ENSP00000430641.1:n.49-4678A=
ENST00000519962.5:c.49-10551A=	ENSP00000429140.1:n.49-10551A=
ENST00000522368.5:c.831A=
ENST00000522394.1:c.123-5947A=	ENSP00000429578.1:n.123-5947A=
ENST00000621845.1:c.500A=	ENSP00000484318.1:p.Asn167=