Canonical Allele Identifier: CA1806686070

Gene: RRM2B

Linked Data

• dbSNP Id: rs1441587875

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231901dup , CM000670.2:g.102231901dup	GRCh38
NC_000008.10:g.103244129dup , CM000670.1:g.103244129dup	GRCh37
NC_000008.9:g.103313305dup	NCBI36
NG_016617.1:g.12225dup , LRG_788:g.12225dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+255dup MANE Select	ENSP00000251810.3:n.204+255dup
ENST00000251810.7:c.204+255dup	ENSP00000251810.3:n.204+255dup
ENST00000395912.6:c.49-5860dup	ENSP00000379248.2:n.49-5860dup
ENST00000517517.1:n.513+255dup
ENST00000519317.5:c.48+6933dup	ENSP00000430641.1:n.48+6933dup
ENST00000519962.5:c.48+6933dup	ENSP00000429140.1:n.48+6933dup
ENST00000522368.5:c.373+255dup
ENST00000522394.1:c.122+337dup	ENSP00000429578.1:n.122+337dup
ENST00000523957.1:c.*127+255dup	ENSP00000427830.1:n.*127+255dup
ENST00000621845.1:c.42+255dup	ENSP00000484318.1:n.42+255dup
NM_001172477.1:c.420+255dup , LRG_788t1:c.420+255dup	NP_001165948.1:n.420+255dup
NM_001172478.1:c.49-5860dup	NP_001165949.1:n.49-5860dup
NM_015713.4:c.204+255dup , LRG_788t2:c.204+255dup	NP_056528.2:n.204+255dup
NM_001172478.2:c.49-5860dup	NP_001165949.1:n.49-5860dup
NM_015713.5:c.204+255dup MANE Select	NP_056528.2:n.204+255dup