Canonical Allele Identifier: CA182479386

Gene: RRM2B

Linked Data

• dbSNP Id: rs965900602
• MyVariant Identifiers: chr8:g.103244191C>T (hg19) ; chr8:g.102231963C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231963C>T , CM000670.2:g.102231963C>T	GRCh38
NC_000008.10:g.103244191C>T , CM000670.1:g.103244191C>T	GRCh37
NC_000008.9:g.103313367C>T	NCBI36
NG_016617.1:g.12156G>A , LRG_788:g.12156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+186G>A MANE Select	ENSP00000251810.3:n.204+186G>A
ENST00000251810.7:c.204+186G>A	ENSP00000251810.3:n.204+186G>A
ENST00000395912.6:c.49-5929G>A	ENSP00000379248.2:n.49-5929G>A
ENST00000517517.1:n.513+186G>A
ENST00000519317.5:c.48+6864G>A	ENSP00000430641.1:n.48+6864G>A
ENST00000519962.5:c.48+6864G>A	ENSP00000429140.1:n.48+6864G>A
ENST00000522368.5:c.373+186G>A
ENST00000522394.1:c.122+268G>A	ENSP00000429578.1:n.122+268G>A
ENST00000523957.1:c.*127+186G>A	ENSP00000427830.1:n.*127+186G>A
ENST00000621845.1:c.42+186G>A	ENSP00000484318.1:n.42+186G>A
NM_001172477.1:c.420+186G>A , LRG_788t1:c.420+186G>A	NP_001165948.1:n.420+186G>A
NM_001172478.1:c.49-5929G>A	NP_001165949.1:n.49-5929G>A
NM_015713.4:c.204+186G>A , LRG_788t2:c.204+186G>A	NP_056528.2:n.204+186G>A
NM_001172478.2:c.49-5929G>A	NP_001165949.1:n.49-5929G>A
NM_015713.5:c.204+186G>A MANE Select	NP_056528.2:n.204+186G>A