Canonical Allele Identifier: CA462123793

Gene: RRM2B

Linked Data

• dbSNP Id: rs2132539484
• COSMIC: COSM6042050
• MyVariant Identifiers: chr8:g.103220442C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208214C>T , CM000670.2:g.102208214C>T	GRCh38
NC_000008.10:g.103220442C>T , CM000670.1:g.103220442C>T	GRCh37
NC_000008.9:g.103289618C>T	NCBI36
NG_016617.1:g.35905G>A , LRG_788:g.35905G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.975G>A MANE Select	ENSP00000251810.3:p.Glu325=
ENST00000251810.7:c.975G>A	ENSP00000251810.3:p.Glu325=
ENST00000395910.6:n.362G>A
ENST00000395912.6:c.819G>A	ENSP00000379248.2:p.Glu273=
ENST00000519317.5:c.339G>A	ENSP00000430641.1:p.Glu113=
ENST00000519962.5:c.120G>A	ENSP00000429140.1:p.Glu40=
ENST00000522368.5:c.1144G>A
ENST00000522394.1:c.308G>A	ENSP00000429578.1:n.308G>A
ENST00000621845.1:c.813G>A	ENSP00000484318.1:p.Glu271=
NM_001172477.1:c.1191G>A , LRG_788t1:c.1191G>A	NP_001165948.1:p.Glu397=
NM_001172478.1:c.819G>A	NP_001165949.1:p.Glu273=
NM_015713.4:c.975G>A , LRG_788t2:c.975G>A	NP_056528.2:p.Glu325=
NM_001172478.2:c.819G>A	NP_001165949.1:p.Glu273=
NM_015713.5:c.975G>A MANE Select	NP_056528.2:p.Glu325=