Canonical Allele Identifier: CA462128508

Gene: RRM2B

Linked Data

• dbSNP Id: rs1316729696
• MyVariant Identifiers: chr8:g.103244476T>C (hg19) ; chr8:g.102232248T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232248T>C , CM000670.2:g.102232248T>C	GRCh38
NC_000008.10:g.103244476T>C , CM000670.1:g.103244476T>C	GRCh37
NC_000008.9:g.103313652T>C	NCBI36
NG_016617.1:g.11871A>G , LRG_788:g.11871A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.105A>G MANE Select	ENSP00000251810.3:p.Leu35=
ENST00000251810.7:c.105A>G	ENSP00000251810.3:p.Leu35=
ENST00000395912.6:c.49-6214A>G	ENSP00000379248.2:n.49-6214A>G
ENST00000517517.1:n.414A>G
ENST00000519317.5:c.48+6579A>G	ENSP00000430641.1:n.48+6579A>G
ENST00000519962.5:c.48+6579A>G	ENSP00000429140.1:n.48+6579A>G
ENST00000522368.5:c.274A>G
ENST00000522394.1:c.105A>G	ENSP00000429578.1:p.Leu35=
ENST00000523957.1:c.*28A>G	ENSP00000427830.1:n.*28A>G
ENST00000621845.1:c.-58A>G	ENSP00000484318.1:n.-58A>G
NM_001172477.1:c.321A>G , LRG_788t1:c.321A>G	NP_001165948.1:p.Leu107=
NM_001172478.1:c.49-6214A>G	NP_001165949.1:n.49-6214A>G
NM_015713.4:c.105A>G , LRG_788t2:c.105A>G	NP_056528.2:p.Leu35=
NM_001172478.2:c.49-6214A>G	NP_001165949.1:n.49-6214A>G
NM_015713.5:c.105A>G MANE Select	NP_056528.2:p.Leu35=