Canonical Allele Identifier: CA1806686142

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232057A= , CM000670.2:g.102232057A=	GRCh38
NC_000008.10:g.103244285A= , CM000670.1:g.103244285A=	GRCh37
NC_000008.9:g.103313461A=	NCBI36
NG_016617.1:g.12062T= , LRG_788:g.12062T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+92T= MANE Select	ENSP00000251810.3:n.204+92T=
ENST00000251810.7:c.204+92T=	ENSP00000251810.3:n.204+92T=
ENST00000395912.6:c.49-6023T=	ENSP00000379248.2:n.49-6023T=
ENST00000517517.1:n.513+92T=
ENST00000519317.5:c.48+6770T=	ENSP00000430641.1:n.48+6770T=
ENST00000519962.5:c.48+6770T=	ENSP00000429140.1:n.48+6770T=
ENST00000522368.5:c.373+92T=
ENST00000522394.1:c.122+174T=	ENSP00000429578.1:n.122+174T=
ENST00000523957.1:c.*127+92T=	ENSP00000427830.1:n.*127+92T=
ENST00000621845.1:c.42+92T=	ENSP00000484318.1:n.42+92T=
NM_001172477.1:c.420+92T= , LRG_788t1:c.420+92T=	NP_001165948.1:n.420+92T=
NM_001172478.1:c.49-6023T=	NP_001165949.1:n.49-6023T=
NM_015713.4:c.204+92T= , LRG_788t2:c.204+92T=	NP_056528.2:n.204+92T=
NM_001172478.2:c.49-6023T=	NP_001165949.1:n.49-6023T=
NM_015713.5:c.204+92T= MANE Select	NP_056528.2:n.204+92T=