Canonical Allele Identifier: CA1806686223

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232232G= , CM000670.2:g.102232232G=	GRCh38
NC_000008.10:g.103244460G= , CM000670.1:g.103244460G=	GRCh37
NC_000008.9:g.103313636G=	NCBI36
NG_016617.1:g.11887C= , LRG_788:g.11887C=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.121C= MANE Select	NP_056528.2:p.Arg41=
ENST00000251810.8:c.121C= MANE Select	ENSP00000251810.3:p.Arg41=
NM_001172477.1:c.337C= , LRG_788t1:c.337C=	NP_001165948.1:p.Arg113=
NM_001172478.1:c.49-6198C=	NP_001165949.1:n.49-6198C=
NM_001172478.2:c.49-6198C=	NP_001165949.1:n.49-6198C=
NM_015713.4:c.121C= , LRG_788t2:c.121C=	NP_056528.2:p.Arg41=
ENST00000251810.7:c.121C=	ENSP00000251810.3:p.Arg41=
ENST00000395912.6:c.49-6198C=	ENSP00000379248.2:n.49-6198C=
ENST00000517517.1:n.430C=
ENST00000519317.5:c.48+6595C=	ENSP00000430641.1:n.48+6595C=
ENST00000519962.5:c.48+6595C=	ENSP00000429140.1:n.48+6595C=
ENST00000522368.5:c.290C=
ENST00000522394.1:c.121C=	ENSP00000429578.1:p.Arg41=
ENST00000523957.1:c.*44C=	ENSP00000427830.1:n.*44C=
ENST00000621845.1:c.-42C=	ENSP00000484318.1:n.-42C=