Canonical Allele Identifier: CA371585168

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220363A>C (hg19) ; chr8:g.102208135A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208135A>C , CM000670.2:g.102208135A>C	GRCh38
NC_000008.10:g.103220363A>C , CM000670.1:g.103220363A>C	GRCh37
NC_000008.9:g.103289539A>C	NCBI36
NG_016617.1:g.35984T>G , LRG_788:g.35984T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.1054T>G MANE Select	ENSP00000251810.3:p.Ter352Glu
ENST00000251810.7:c.1054T>G	ENSP00000251810.3:p.Ter352Glu
ENST00000395910.6:n.441T>G
ENST00000395912.6:c.898T>G	ENSP00000379248.2:p.Ter300Glu
ENST00000519317.5:c.418T>G	ENSP00000430641.1:p.Ter140Glu
ENST00000519962.5:c.199T>G	ENSP00000429140.1:p.Ter67Glu
ENST00000522368.5:c.1223T>G
ENST00000522394.1:c.387T>G	ENSP00000429578.1:n.387T>G
ENST00000621845.1:c.892T>G	ENSP00000484318.1:p.Ter298Glu
NM_001172477.1:c.1270T>G , LRG_788t1:c.1270T>G	NP_001165948.1:p.Ter424Glu
NM_001172478.1:c.898T>G	NP_001165949.1:p.Ter300Glu
NM_015713.4:c.1054T>G , LRG_788t2:c.1054T>G	NP_056528.2:p.Ter352Glu
NM_001172478.2:c.898T>G	NP_001165949.1:p.Ter300Glu
NM_015713.5:c.1054T>G MANE Select	NP_056528.2:p.Ter352Glu