Canonical Allele Identifier: CA462123907

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220469A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208241A>C , CM000670.2:g.102208241A>C	GRCh38
NC_000008.10:g.103220469A>C , CM000670.1:g.103220469A>C	GRCh37
NC_000008.9:g.103289645A>C	NCBI36
NG_016617.1:g.35878T>G , LRG_788:g.35878T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.948T>G MANE Select	ENSP00000251810.3:p.Ser316=
ENST00000251810.7:c.948T>G	ENSP00000251810.3:p.Ser316=
ENST00000395910.6:n.335T>G
ENST00000395912.6:c.792T>G	ENSP00000379248.2:p.Ser264=
ENST00000519317.5:c.312T>G	ENSP00000430641.1:p.Ser104=
ENST00000519962.5:c.93T>G	ENSP00000429140.1:p.Ser31=
ENST00000522368.5:c.1117T>G
ENST00000522394.1:c.281T>G	ENSP00000429578.1:n.281T>G
ENST00000621845.1:c.786T>G	ENSP00000484318.1:p.Ser262=
NM_001172477.1:c.1164T>G , LRG_788t1:c.1164T>G	NP_001165948.1:p.Ser388=
NM_001172478.1:c.792T>G	NP_001165949.1:p.Ser264=
NM_015713.4:c.948T>G , LRG_788t2:c.948T>G	NP_056528.2:p.Ser316=
NM_001172478.2:c.792T>G	NP_001165949.1:p.Ser264=
NM_015713.5:c.948T>G MANE Select	NP_056528.2:p.Ser316=