Canonical Allele Identifier: CA371590527

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103231171T>G (hg19) ; chr8:g.102218943T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218943T>G , CM000670.2:g.102218943T>G	GRCh38
NC_000008.10:g.103231171T>G , CM000670.1:g.103231171T>G	GRCh37
NC_000008.9:g.103300347T>G	NCBI36
NG_016617.1:g.25176A>C , LRG_788:g.25176A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.555A>C MANE Select	ENSP00000251810.3:p.Glu185Asp
ENST00000251810.7:c.555A>C	ENSP00000251810.3:p.Glu185Asp
ENST00000395912.6:c.399A>C	ENSP00000379248.2:p.Glu133Asp
ENST00000519125.1:n.73A>C
ENST00000519317.5:c.49-4785A>C	ENSP00000430641.1:n.49-4785A>C
ENST00000519962.5:c.49-10658A>C	ENSP00000429140.1:n.49-10658A>C
ENST00000522368.5:c.724A>C
ENST00000522394.1:c.123-6054A>C	ENSP00000429578.1:n.123-6054A>C
ENST00000621845.1:c.393A>C	ENSP00000484318.1:p.Glu131Asp
NM_001172477.1:c.771A>C , LRG_788t1:c.771A>C	NP_001165948.1:p.Glu257Asp
NM_001172478.1:c.399A>C	NP_001165949.1:p.Glu133Asp
NM_015713.4:c.555A>C , LRG_788t2:c.555A>C	NP_056528.2:p.Glu185Asp
NM_001172478.2:c.399A>C	NP_001165949.1:p.Glu133Asp
NM_015713.5:c.555A>C MANE Select	NP_056528.2:p.Glu185Asp