Canonical Allele Identifier: CA462128440

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102232152-T-C
• MyVariant Identifiers: chr8:g.103244380T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232152T>C , CM000670.2:g.102232152T>C	GRCh38
NC_000008.10:g.103244380T>C , CM000670.1:g.103244380T>C	GRCh37
NC_000008.9:g.103313556T>C	NCBI36
NG_016617.1:g.11967A>G , LRG_788:g.11967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.201A>G MANE Select	ENSP00000251810.3:p.Glu67=
ENST00000251810.7:c.201A>G	ENSP00000251810.3:p.Glu67=
ENST00000395912.6:c.49-6118A>G	ENSP00000379248.2:n.49-6118A>G
ENST00000517517.1:n.510A>G
ENST00000519317.5:c.48+6675A>G	ENSP00000430641.1:n.48+6675A>G
ENST00000519962.5:c.48+6675A>G	ENSP00000429140.1:n.48+6675A>G
ENST00000522368.5:c.370A>G
ENST00000522394.1:c.122+79A>G	ENSP00000429578.1:n.122+79A>G
ENST00000523957.1:c.*124A>G	ENSP00000427830.1:n.*124A>G
ENST00000621845.1:c.39A>G	ENSP00000484318.1:p.Glu13=
NM_001172477.1:c.417A>G , LRG_788t1:c.417A>G	NP_001165948.1:p.Glu139=
NM_001172478.1:c.49-6118A>G	NP_001165949.1:n.49-6118A>G
NM_015713.4:c.201A>G , LRG_788t2:c.201A>G	NP_056528.2:p.Glu67=
NM_001172478.2:c.49-6118A>G	NP_001165949.1:n.49-6118A>G
NM_015713.5:c.201A>G MANE Select	NP_056528.2:p.Glu67=