Canonical Allele Identifier: CA1806678340

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218915C= , CM000670.2:g.102218915C=	GRCh38
NC_000008.10:g.103231143C= , CM000670.1:g.103231143C=	GRCh37
NC_000008.9:g.103300319C=	NCBI36
NG_016617.1:g.25204G= , LRG_788:g.25204G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.583G= MANE Select	NP_056528.2:p.Gly195=
ENST00000251810.8:c.583G= MANE Select	ENSP00000251810.3:p.Gly195=
NM_001172477.1:c.799G= , LRG_788t1:c.799G=	NP_001165948.1:p.Gly267=
NM_001172478.1:c.427G=	NP_001165949.1:p.Gly143=
NM_001172478.2:c.427G=	NP_001165949.1:p.Gly143=
NM_015713.4:c.583G= , LRG_788t2:c.583G=	NP_056528.2:p.Gly195=
ENST00000251810.7:c.583G=	ENSP00000251810.3:p.Gly195=
ENST00000395912.6:c.427G=	ENSP00000379248.2:p.Gly143=
ENST00000519125.1:n.101G=
ENST00000519317.5:c.49-4757G=	ENSP00000430641.1:n.49-4757G=
ENST00000519962.5:c.49-10630G=	ENSP00000429140.1:n.49-10630G=
ENST00000522368.5:c.752G=
ENST00000522394.1:c.123-6026G=	ENSP00000429578.1:n.123-6026G=
ENST00000621845.1:c.421G=	ENSP00000484318.1:p.Gly141=