Canonical Allele Identifier: CA371596215

Gene: RRM2B

Linked Data

• COSMIC: COSM1094388
• MyVariant Identifiers: chr8:g.103244465G>T (hg19) ; chr8:g.102232237G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232237G>T , CM000670.2:g.102232237G>T	GRCh38
NC_000008.10:g.103244465G>T , CM000670.1:g.103244465G>T	GRCh37
NC_000008.9:g.103313641G>T	NCBI36
NG_016617.1:g.11882C>A , LRG_788:g.11882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.116C>A MANE Select	ENSP00000251810.3:p.Ser39Tyr
ENST00000251810.7:c.116C>A	ENSP00000251810.3:p.Ser39Tyr
ENST00000395912.6:c.49-6203C>A	ENSP00000379248.2:n.49-6203C>A
ENST00000517517.1:n.425C>A
ENST00000519317.5:c.48+6590C>A	ENSP00000430641.1:n.48+6590C>A
ENST00000519962.5:c.48+6590C>A	ENSP00000429140.1:n.48+6590C>A
ENST00000522368.5:c.285C>A
ENST00000522394.1:c.116C>A	ENSP00000429578.1:p.Ser39Tyr
ENST00000523957.1:c.*39C>A	ENSP00000427830.1:n.*39C>A
ENST00000621845.1:c.-47C>A	ENSP00000484318.1:n.-47C>A
NM_001172477.1:c.332C>A , LRG_788t1:c.332C>A	NP_001165948.1:p.Ser111Tyr
NM_001172478.1:c.49-6203C>A	NP_001165949.1:n.49-6203C>A
NM_015713.4:c.116C>A , LRG_788t2:c.116C>A	NP_056528.2:p.Ser39Tyr
NM_001172478.2:c.49-6203C>A	NP_001165949.1:n.49-6203C>A
NM_015713.5:c.116C>A MANE Select	NP_056528.2:p.Ser39Tyr