Canonical Allele Identifier: CA1806681654

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224909G= , CM000670.2:g.102224909G=	GRCh38
NC_000008.10:g.103237137G= , CM000670.1:g.103237137G=	GRCh37
NC_000008.9:g.103306313G=	NCBI36
NG_016617.1:g.19210C= , LRG_788:g.19210C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.431C= MANE Select	NP_056528.2:p.Thr144=
ENST00000251810.8:c.431C= MANE Select	ENSP00000251810.3:p.Thr144=
NM_001172477.1:c.647C= , LRG_788t1:c.647C=	NP_001165948.1:p.Thr216=
NM_001172478.1:c.275C=	NP_001165949.1:p.Thr92=
NM_001172478.2:c.275C=	NP_001165949.1:p.Thr92=
NM_015713.4:c.431C= , LRG_788t2:c.431C=	NP_056528.2:p.Thr144=
ENST00000251810.7:c.431C=	ENSP00000251810.3:p.Thr144=
ENST00000395912.6:c.275C=	ENSP00000379248.2:p.Thr92=
ENST00000519317.5:c.49-10751C=	ENSP00000430641.1:n.49-10751C=
ENST00000519962.5:c.48+13918C=	ENSP00000429140.1:n.48+13918C=
ENST00000522368.5:c.600C=
ENST00000522394.1:c.122+7322C=	ENSP00000429578.1:n.122+7322C=
ENST00000621845.1:c.269C=	ENSP00000484318.1:p.Thr90=