Canonical Allele Identifier: CA462127631

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237114T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224886T>G , CM000670.2:g.102224886T>G	GRCh38
NC_000008.10:g.103237114T>G , CM000670.1:g.103237114T>G	GRCh37
NC_000008.9:g.103306290T>G	NCBI36
NG_016617.1:g.19233A>C , LRG_788:g.19233A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.454A>C MANE Select	ENSP00000251810.3:p.Arg152=
ENST00000251810.7:c.454A>C	ENSP00000251810.3:p.Arg152=
ENST00000395912.6:c.298A>C	ENSP00000379248.2:p.Arg100=
ENST00000519317.5:c.49-10728A>C	ENSP00000430641.1:n.49-10728A>C
ENST00000519962.5:c.48+13941A>C	ENSP00000429140.1:n.48+13941A>C
ENST00000522368.5:c.623A>C
ENST00000522394.1:c.122+7345A>C	ENSP00000429578.1:n.122+7345A>C
ENST00000621845.1:c.292A>C	ENSP00000484318.1:p.Arg98=
NM_001172477.1:c.670A>C , LRG_788t1:c.670A>C	NP_001165948.1:p.Arg224=
NM_001172478.1:c.298A>C	NP_001165949.1:p.Arg100=
NM_015713.4:c.454A>C , LRG_788t2:c.454A>C	NP_056528.2:p.Arg152=
NM_001172478.2:c.298A>C	NP_001165949.1:p.Arg100=
NM_015713.5:c.454A>C MANE Select	NP_056528.2:p.Arg152=