Canonical Allele Identifier: CA1806676553

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102212829G= , CM000670.2:g.102212829G=	GRCh38
NC_000008.10:g.103225057G= , CM000670.1:g.103225057G=	GRCh37
NC_000008.9:g.103294233G=	NCBI36
NG_016617.1:g.31290C= , LRG_788:g.31290C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.850C= MANE Select	NP_056528.2:p.Gln284=
ENST00000251810.8:c.850C= MANE Select	ENSP00000251810.3:p.Gln284=
NM_001172477.1:c.1066C= , LRG_788t1:c.1066C=	NP_001165948.1:p.Gln356=
NM_001172478.1:c.694C=	NP_001165949.1:p.Gln232=
NM_001172478.2:c.694C=	NP_001165949.1:p.Gln232=
NM_015713.4:c.850C= , LRG_788t2:c.850C=	NP_056528.2:p.Gln284=
ENST00000251810.7:c.850C=	ENSP00000251810.3:p.Gln284=
ENST00000395910.6:n.237C=
ENST00000395912.6:c.694C=	ENSP00000379248.2:p.Gln232=
ENST00000519125.1:n.368C=
ENST00000519317.5:c.214C=	ENSP00000430641.1:p.Gln72=
ENST00000519962.5:c.49-4544C=	ENSP00000429140.1:n.49-4544C=
ENST00000522368.5:c.1019C=
ENST00000522394.1:c.183C=	ENSP00000429578.1:n.183C=
ENST00000621845.1:c.688C=	ENSP00000484318.1:p.Gln230=