Canonical Allele Identifier: CA1806686060

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811035884

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231884_102231885insGA , CM000670.2:g.102231884_102231885insGA	GRCh38
NC_000008.10:g.103244112_103244113insGA , CM000670.1:g.103244112_103244113insGA	GRCh37
NC_000008.9:g.103313288_103313289insGA	NCBI36
NG_016617.1:g.12235_12236insCT , LRG_788:g.12235_12236insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+265_204+266insCT MANE Select	ENSP00000251810.3:n.204+265_204+266insCT
ENST00000251810.7:c.204+265_204+266insCT	ENSP00000251810.3:n.204+265_204+266insCT
ENST00000395912.6:c.49-5850_49-5849insCT	ENSP00000379248.2:n.49-5850_49-5849insCT
ENST00000517517.1:n.513+265_513+266insCT
ENST00000519317.5:c.48+6943_48+6944insCT	ENSP00000430641.1:n.48+6943_48+6944insCT
ENST00000519962.5:c.48+6943_48+6944insCT	ENSP00000429140.1:n.48+6943_48+6944insCT
ENST00000522368.5:c.373+265_373+266insCT
ENST00000522394.1:c.122+347_122+348insCT	ENSP00000429578.1:n.122+347_122+348insCT
ENST00000523957.1:c.*127+265_*127+266insCT	ENSP00000427830.1:n.*127+265_*127+266insCT
ENST00000621845.1:c.42+265_42+266insCT	ENSP00000484318.1:n.42+265_42+266insCT
NM_001172477.1:c.420+265_420+266insCT , LRG_788t1:c.420+265_420+266insCT	NP_001165948.1:n.420+265_420+266insCT
NM_001172478.1:c.49-5850_49-5849insCT	NP_001165949.1:n.49-5850_49-5849insCT
NM_015713.4:c.204+265_204+266insCT , LRG_788t2:c.204+265_204+266insCT	NP_056528.2:n.204+265_204+266insCT
NM_001172478.2:c.49-5850_49-5849insCT	NP_001165949.1:n.49-5850_49-5849insCT
NM_015713.5:c.204+265_204+266insCT MANE Select	NP_056528.2:n.204+265_204+266insCT