Canonical Allele Identifier: CA371592161

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237111A>G (hg19) ; chr8:g.102224883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224883A>G , CM000670.2:g.102224883A>G	GRCh38
NC_000008.10:g.103237111A>G , CM000670.1:g.103237111A>G	GRCh37
NC_000008.9:g.103306287A>G	NCBI36
NG_016617.1:g.19236T>C , LRG_788:g.19236T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.455+2T>C MANE Select	ENSP00000251810.3:n.455+2T>C
ENST00000251810.7:c.455+2T>C	ENSP00000251810.3:n.455+2T>C
ENST00000395912.6:c.299+2T>C	ENSP00000379248.2:n.299+2T>C
ENST00000519317.5:c.49-10725T>C	ENSP00000430641.1:n.49-10725T>C
ENST00000519962.5:c.48+13944T>C	ENSP00000429140.1:n.48+13944T>C
ENST00000522368.5:c.624+2T>C
ENST00000522394.1:c.122+7348T>C	ENSP00000429578.1:n.122+7348T>C
ENST00000621845.1:c.293+2T>C	ENSP00000484318.1:n.293+2T>C
NM_001172477.1:c.671+2T>C , LRG_788t1:c.671+2T>C	NP_001165948.1:n.671+2T>C
NM_001172478.1:c.299+2T>C	NP_001165949.1:n.299+2T>C
NM_015713.4:c.455+2T>C , LRG_788t2:c.455+2T>C	NP_056528.2:n.455+2T>C
NM_001172478.2:c.299+2T>C	NP_001165949.1:n.299+2T>C
NM_015713.5:c.455+2T>C MANE Select	NP_056528.2:n.455+2T>C