Canonical Allele Identifier: CA371585306

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220392T>C (hg19) ; chr8:g.102208164T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208164T>C , CM000670.2:g.102208164T>C	GRCh38
NC_000008.10:g.103220392T>C , CM000670.1:g.103220392T>C	GRCh37
NC_000008.9:g.103289568T>C	NCBI36
NG_016617.1:g.35955A>G , LRG_788:g.35955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1025A>G MANE Select	ENSP00000251810.3:p.Asp342Gly
ENST00000251810.7:c.1025A>G	ENSP00000251810.3:p.Asp342Gly
ENST00000395910.6:n.412A>G
ENST00000395912.6:c.869A>G	ENSP00000379248.2:p.Asp290Gly
ENST00000519317.5:c.389A>G	ENSP00000430641.1:p.Asp130Gly
ENST00000519962.5:c.170A>G	ENSP00000429140.1:p.Asp57Gly
ENST00000522368.5:c.1194A>G
ENST00000522394.1:c.358A>G	ENSP00000429578.1:n.358A>G
ENST00000621845.1:c.863A>G	ENSP00000484318.1:p.Asp288Gly
NM_001172477.1:c.1241A>G , LRG_788t1:c.1241A>G	NP_001165948.1:p.Asp414Gly
NM_001172478.1:c.869A>G	NP_001165949.1:p.Asp290Gly
NM_015713.4:c.1025A>G , LRG_788t2:c.1025A>G	NP_056528.2:p.Asp342Gly
NM_001172478.2:c.869A>G	NP_001165949.1:p.Asp290Gly
NM_015713.5:c.1025A>G MANE Select	NP_056528.2:p.Asp342Gly