Canonical Allele Identifier: CA1806682601

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102226036T= , CM000670.2:g.102226036T=	GRCh38
NC_000008.10:g.103238264T= , CM000670.1:g.103238264T=	GRCh37
NC_000008.9:g.103307440T=	NCBI36
NG_016617.1:g.18083A= , LRG_788:g.18083A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.205-2A= MANE Select	ENSP00000251810.3:n.205-2A=
ENST00000251810.7:c.205-2A=	ENSP00000251810.3:n.205-2A=
ENST00000395912.6:c.49-2A=	ENSP00000379248.2:n.49-2A=
ENST00000517517.1:n.514-2A=
ENST00000519317.5:c.49-11878A=	ENSP00000430641.1:n.49-11878A=
ENST00000519962.5:c.48+12791A=	ENSP00000429140.1:n.48+12791A=
ENST00000522368.5:c.374-2A=
ENST00000522394.1:c.122+6195A=	ENSP00000429578.1:n.122+6195A=
ENST00000523957.1:c.*128-2A=	ENSP00000427830.1:n.*128-2A=
ENST00000621845.1:c.43-2A=	ENSP00000484318.1:n.43-2A=
NM_001172477.1:c.421-2A= , LRG_788t1:c.421-2A=	NP_001165948.1:n.421-2A=
NM_001172478.1:c.49-2A=	NP_001165949.1:n.49-2A=
NM_015713.4:c.205-2A= , LRG_788t2:c.205-2A=	NP_056528.2:n.205-2A=
NM_001172478.2:c.49-2A=	NP_001165949.1:n.49-2A=
NM_015713.5:c.205-2A= MANE Select	NP_056528.2:n.205-2A=