Canonical Allele Identifier: CA371592194

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237117T>C (hg19) ; chr8:g.102224889T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224889T>C , CM000670.2:g.102224889T>C	GRCh38
NC_000008.10:g.103237117T>C , CM000670.1:g.103237117T>C	GRCh37
NC_000008.9:g.103306293T>C	NCBI36
NG_016617.1:g.19230A>G , LRG_788:g.19230A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.451A>G MANE Select	ENSP00000251810.3:p.Lys151Glu
ENST00000251810.7:c.451A>G	ENSP00000251810.3:p.Lys151Glu
ENST00000395912.6:c.295A>G	ENSP00000379248.2:p.Lys99Glu
ENST00000519317.5:c.49-10731A>G	ENSP00000430641.1:n.49-10731A>G
ENST00000519962.5:c.48+13938A>G	ENSP00000429140.1:n.48+13938A>G
ENST00000522368.5:c.620A>G
ENST00000522394.1:c.122+7342A>G	ENSP00000429578.1:n.122+7342A>G
ENST00000621845.1:c.289A>G	ENSP00000484318.1:p.Lys97Glu
NM_001172477.1:c.667A>G , LRG_788t1:c.667A>G	NP_001165948.1:p.Lys223Glu
NM_001172478.1:c.295A>G	NP_001165949.1:p.Lys99Glu
NM_015713.4:c.451A>G , LRG_788t2:c.451A>G	NP_056528.2:p.Lys151Glu
NM_001172478.2:c.295A>G	NP_001165949.1:p.Lys99Glu
NM_015713.5:c.451A>G MANE Select	NP_056528.2:p.Lys151Glu