Canonical Allele Identifier: CA1806686098

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231960A= , CM000670.2:g.102231960A=	GRCh38
NC_000008.10:g.103244188A= , CM000670.1:g.103244188A=	GRCh37
NC_000008.9:g.103313364A=	NCBI36
NG_016617.1:g.12159T= , LRG_788:g.12159T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+189T= MANE Select	ENSP00000251810.3:n.204+189T=
ENST00000251810.7:c.204+189T=	ENSP00000251810.3:n.204+189T=
ENST00000395912.6:c.49-5926T=	ENSP00000379248.2:n.49-5926T=
ENST00000517517.1:n.513+189T=
ENST00000519317.5:c.48+6867T=	ENSP00000430641.1:n.48+6867T=
ENST00000519962.5:c.48+6867T=	ENSP00000429140.1:n.48+6867T=
ENST00000522368.5:c.373+189T=
ENST00000522394.1:c.122+271T=	ENSP00000429578.1:n.122+271T=
ENST00000523957.1:c.*127+189T=	ENSP00000427830.1:n.*127+189T=
ENST00000621845.1:c.42+189T=	ENSP00000484318.1:n.42+189T=
NM_001172477.1:c.420+189T= , LRG_788t1:c.420+189T=	NP_001165948.1:n.420+189T=
NM_001172478.1:c.49-5926T=	NP_001165949.1:n.49-5926T=
NM_015713.4:c.204+189T= , LRG_788t2:c.204+189T=	NP_056528.2:n.204+189T=
NM_001172478.2:c.49-5926T=	NP_001165949.1:n.49-5926T=
NM_015713.5:c.204+189T= MANE Select	NP_056528.2:n.204+189T=