Canonical Allele Identifier: CA462127728

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237214T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224986T>C , CM000670.2:g.102224986T>C	GRCh38
NC_000008.10:g.103237214T>C , CM000670.1:g.103237214T>C	GRCh37
NC_000008.9:g.103306390T>C	NCBI36
NG_016617.1:g.19133A>G , LRG_788:g.19133A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.354A>G MANE Select	ENSP00000251810.3:p.Pro118=
ENST00000251810.7:c.354A>G	ENSP00000251810.3:p.Pro118=
ENST00000395912.6:c.198A>G	ENSP00000379248.2:p.Pro66=
ENST00000519317.5:c.49-10828A>G	ENSP00000430641.1:n.49-10828A>G
ENST00000519962.5:c.48+13841A>G	ENSP00000429140.1:n.48+13841A>G
ENST00000522368.5:c.523A>G
ENST00000522394.1:c.122+7245A>G	ENSP00000429578.1:n.122+7245A>G
ENST00000523957.1:c.*277A>G	ENSP00000427830.1:n.*277A>G
ENST00000621845.1:c.192A>G	ENSP00000484318.1:p.Pro64=
NM_001172477.1:c.570A>G , LRG_788t1:c.570A>G	NP_001165948.1:p.Pro190=
NM_001172478.1:c.198A>G	NP_001165949.1:p.Pro66=
NM_015713.4:c.354A>G , LRG_788t2:c.354A>G	NP_056528.2:p.Pro118=
NM_001172478.2:c.198A>G	NP_001165949.1:p.Pro66=
NM_015713.5:c.354A>G MANE Select	NP_056528.2:p.Pro118=