Canonical Allele Identifier: CA1806686043

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811034717

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231866_102231867insA , CM000670.2:g.102231866_102231867insA	GRCh38
NC_000008.10:g.103244094_103244095insA , CM000670.1:g.103244094_103244095insA	GRCh37
NC_000008.9:g.103313270_103313271insA	NCBI36
NG_016617.1:g.12252_12253insT , LRG_788:g.12252_12253insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+282_204+283insT MANE Select	ENSP00000251810.3:n.204+282_204+283insT
ENST00000251810.7:c.204+282_204+283insT	ENSP00000251810.3:n.204+282_204+283insT
ENST00000395912.6:c.49-5833_49-5832insT	ENSP00000379248.2:n.49-5833_49-5832insT
ENST00000517517.1:n.513+282_513+283insT
ENST00000519317.5:c.48+6960_48+6961insT	ENSP00000430641.1:n.48+6960_48+6961insT
ENST00000519962.5:c.48+6960_48+6961insT	ENSP00000429140.1:n.48+6960_48+6961insT
ENST00000522368.5:c.373+282_373+283insT
ENST00000522394.1:c.122+364_122+365insT	ENSP00000429578.1:n.122+364_122+365insT
ENST00000523957.1:c.*127+282_*127+283insT	ENSP00000427830.1:n.*127+282_*127+283insT
ENST00000621845.1:c.42+282_42+283insT	ENSP00000484318.1:n.42+282_42+283insT
NM_001172477.1:c.420+282_420+283insT , LRG_788t1:c.420+282_420+283insT	NP_001165948.1:n.420+282_420+283insT
NM_001172478.1:c.49-5833_49-5832insT	NP_001165949.1:n.49-5833_49-5832insT
NM_015713.4:c.204+282_204+283insT , LRG_788t2:c.204+282_204+283insT	NP_056528.2:n.204+282_204+283insT
NM_001172478.2:c.49-5833_49-5832insT	NP_001165949.1:n.49-5833_49-5832insT
NM_015713.5:c.204+282_204+283insT MANE Select	NP_056528.2:n.204+282_204+283insT