Canonical Allele Identifier: CA1806686233

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232256G= , CM000670.2:g.102232256G=	GRCh38
NC_000008.10:g.103244484G= , CM000670.1:g.103244484G=	GRCh37
NC_000008.9:g.103313660G=	NCBI36
NG_016617.1:g.11863C= , LRG_788:g.11863C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.97C= MANE Select	ENSP00000251810.3:p.Pro33=
ENST00000251810.7:c.97C=	ENSP00000251810.3:p.Pro33=
ENST00000395912.6:c.49-6222C=	ENSP00000379248.2:n.49-6222C=
ENST00000517517.1:n.406C=
ENST00000519317.5:c.48+6571C=	ENSP00000430641.1:n.48+6571C=
ENST00000519962.5:c.48+6571C=	ENSP00000429140.1:n.48+6571C=
ENST00000522368.5:c.266C=
ENST00000522394.1:c.97C=	ENSP00000429578.1:p.Pro33=
ENST00000523957.1:c.*20C=	ENSP00000427830.1:n.*20C=
ENST00000621845.1:c.-66C=	ENSP00000484318.1:n.-66C=
NM_001172477.1:c.313C= , LRG_788t1:c.313C=	NP_001165948.1:p.Pro105=
NM_001172478.1:c.49-6222C=	NP_001165949.1:n.49-6222C=
NM_015713.4:c.97C= , LRG_788t2:c.97C=	NP_056528.2:p.Pro33=
NM_001172478.2:c.49-6222C=	NP_001165949.1:n.49-6222C=
NM_015713.5:c.97C= MANE Select	NP_056528.2:p.Pro33=