Canonical Allele Identifier: CA371590531

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103231172T>G (hg19) ; chr8:g.102218944T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218944T>G , CM000670.2:g.102218944T>G	GRCh38
NC_000008.10:g.103231172T>G , CM000670.1:g.103231172T>G	GRCh37
NC_000008.9:g.103300348T>G	NCBI36
NG_016617.1:g.25175A>C , LRG_788:g.25175A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.554A>C MANE Select	ENSP00000251810.3:p.Glu185Ala
ENST00000251810.7:c.554A>C	ENSP00000251810.3:p.Glu185Ala
ENST00000395912.6:c.398A>C	ENSP00000379248.2:p.Glu133Ala
ENST00000519125.1:n.72A>C
ENST00000519317.5:c.49-4786A>C	ENSP00000430641.1:n.49-4786A>C
ENST00000519962.5:c.49-10659A>C	ENSP00000429140.1:n.49-10659A>C
ENST00000522368.5:c.723A>C
ENST00000522394.1:c.123-6055A>C	ENSP00000429578.1:n.123-6055A>C
ENST00000621845.1:c.392A>C	ENSP00000484318.1:p.Glu131Ala
NM_001172477.1:c.770A>C , LRG_788t1:c.770A>C	NP_001165948.1:p.Glu257Ala
NM_001172478.1:c.398A>C	NP_001165949.1:p.Glu133Ala
NM_015713.4:c.554A>C , LRG_788t2:c.554A>C	NP_056528.2:p.Glu185Ala
NM_001172478.2:c.398A>C	NP_001165949.1:p.Glu133Ala
NM_015713.5:c.554A>C MANE Select	NP_056528.2:p.Glu185Ala