Canonical Allele Identifier: CA1806686033

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231857A= , CM000670.2:g.102231857A=	GRCh38
NC_000008.10:g.103244085A= , CM000670.1:g.103244085A=	GRCh37
NC_000008.9:g.103313261A=	NCBI36
NG_016617.1:g.12262T= , LRG_788:g.12262T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+292T= MANE Select	ENSP00000251810.3:n.204+292T=
ENST00000251810.7:c.204+292T=	ENSP00000251810.3:n.204+292T=
ENST00000395912.6:c.49-5823T=	ENSP00000379248.2:n.49-5823T=
ENST00000517517.1:n.513+292T=
ENST00000519317.5:c.48+6970T=	ENSP00000430641.1:n.48+6970T=
ENST00000519962.5:c.48+6970T=	ENSP00000429140.1:n.48+6970T=
ENST00000522368.5:c.373+292T=
ENST00000522394.1:c.122+374T=	ENSP00000429578.1:n.122+374T=
ENST00000523957.1:c.*127+292T=	ENSP00000427830.1:n.*127+292T=
ENST00000621845.1:c.42+292T=	ENSP00000484318.1:n.42+292T=
NM_001172477.1:c.420+292T= , LRG_788t1:c.420+292T=	NP_001165948.1:n.420+292T=
NM_001172478.1:c.49-5823T=	NP_001165949.1:n.49-5823T=
NM_015713.4:c.204+292T= , LRG_788t2:c.204+292T=	NP_056528.2:n.204+292T=
NM_001172478.2:c.49-5823T=	NP_001165949.1:n.49-5823T=
NM_015713.5:c.204+292T= MANE Select	NP_056528.2:n.204+292T=