Canonical Allele Identifier: CA371595871

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103244397A>T (hg19) ; chr8:g.102232169A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232169A>T , CM000670.2:g.102232169A>T	GRCh38
NC_000008.10:g.103244397A>T , CM000670.1:g.103244397A>T	GRCh37
NC_000008.9:g.103313573A>T	NCBI36
NG_016617.1:g.11950T>A , LRG_788:g.11950T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.184T>A MANE Select	ENSP00000251810.3:p.Ser62Thr
ENST00000251810.7:c.184T>A	ENSP00000251810.3:p.Ser62Thr
ENST00000395912.6:c.49-6135T>A	ENSP00000379248.2:n.49-6135T>A
ENST00000517517.1:n.493T>A
ENST00000519317.5:c.48+6658T>A	ENSP00000430641.1:n.48+6658T>A
ENST00000519962.5:c.48+6658T>A	ENSP00000429140.1:n.48+6658T>A
ENST00000522368.5:c.353T>A
ENST00000522394.1:c.122+62T>A	ENSP00000429578.1:n.122+62T>A
ENST00000523957.1:c.*107T>A	ENSP00000427830.1:n.*107T>A
ENST00000621845.1:c.22T>A	ENSP00000484318.1:p.Ser8Thr
NM_001172477.1:c.400T>A , LRG_788t1:c.400T>A	NP_001165948.1:p.Ser134Thr
NM_001172478.1:c.49-6135T>A	NP_001165949.1:n.49-6135T>A
NM_015713.4:c.184T>A , LRG_788t2:c.184T>A	NP_056528.2:p.Ser62Thr
NM_001172478.2:c.49-6135T>A	NP_001165949.1:n.49-6135T>A
NM_015713.5:c.184T>A MANE Select	NP_056528.2:p.Ser62Thr