Canonical Allele Identifier: CA1806682587

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102226031C= , CM000670.2:g.102226031C=	GRCh38
NC_000008.10:g.103238259C= , CM000670.1:g.103238259C=	GRCh37
NC_000008.9:g.103307435C=	NCBI36
NG_016617.1:g.18088G= , LRG_788:g.18088G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.208G= MANE Select	ENSP00000251810.3:p.Asp70=
ENST00000251810.7:c.208G=	ENSP00000251810.3:p.Asp70=
ENST00000395912.6:c.52G=	ENSP00000379248.2:p.Asp18=
ENST00000517517.1:n.517G=
ENST00000519317.5:c.49-11873G=	ENSP00000430641.1:n.49-11873G=
ENST00000519962.5:c.48+12796G=	ENSP00000429140.1:n.48+12796G=
ENST00000522368.5:c.377G=
ENST00000522394.1:c.122+6200G=	ENSP00000429578.1:n.122+6200G=
ENST00000523957.1:c.*131G=	ENSP00000427830.1:n.*131G=
ENST00000621845.1:c.46G=	ENSP00000484318.1:p.Asp16=
NM_001172477.1:c.424G= , LRG_788t1:c.424G=	NP_001165948.1:p.Asp142=
NM_001172478.1:c.52G=	NP_001165949.1:p.Asp18=
NM_015713.4:c.208G= , LRG_788t2:c.208G=	NP_056528.2:p.Asp70=
NM_001172478.2:c.52G=	NP_001165949.1:p.Asp18=
NM_015713.5:c.208G= MANE Select	NP_056528.2:p.Asp70=