Canonical Allele Identifier: CA182475627

Gene: RRM2B

Linked Data

• dbSNP Id: rs747172692
• gnomAD v4: 8-102224882-T-C
• MyVariant Identifiers: chr8:g.103237110T>C (hg19) ; chr8:g.102224882T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224882T>C , CM000670.2:g.102224882T>C	GRCh38
NC_000008.10:g.103237110T>C , CM000670.1:g.103237110T>C	GRCh37
NC_000008.9:g.103306286T>C	NCBI36
NG_016617.1:g.19237A>G , LRG_788:g.19237A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.455+3A>G MANE Select	ENSP00000251810.3:n.455+3A>G
ENST00000251810.7:c.455+3A>G	ENSP00000251810.3:n.455+3A>G
ENST00000395912.6:c.299+3A>G	ENSP00000379248.2:n.299+3A>G
ENST00000519317.5:c.49-10724A>G	ENSP00000430641.1:n.49-10724A>G
ENST00000519962.5:c.48+13945A>G	ENSP00000429140.1:n.48+13945A>G
ENST00000522368.5:c.624+3A>G
ENST00000522394.1:c.122+7349A>G	ENSP00000429578.1:n.122+7349A>G
ENST00000621845.1:c.293+3A>G	ENSP00000484318.1:n.293+3A>G
NM_001172477.1:c.671+3A>G , LRG_788t1:c.671+3A>G	NP_001165948.1:n.671+3A>G
NM_001172478.1:c.299+3A>G	NP_001165949.1:n.299+3A>G
NM_015713.4:c.455+3A>G , LRG_788t2:c.455+3A>G	NP_056528.2:n.455+3A>G
NM_001172478.2:c.299+3A>G	NP_001165949.1:n.299+3A>G
NM_015713.5:c.455+3A>G MANE Select	NP_056528.2:n.455+3A>G