Canonical Allele Identifier: CA1806686138

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811039354

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232049T>A , CM000670.2:g.102232049T>A	GRCh38
NC_000008.10:g.103244277T>A , CM000670.1:g.103244277T>A	GRCh37
NC_000008.9:g.103313453T>A	NCBI36
NG_016617.1:g.12070A>T , LRG_788:g.12070A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+100A>T MANE Select	ENSP00000251810.3:n.204+100A>T
ENST00000251810.7:c.204+100A>T	ENSP00000251810.3:n.204+100A>T
ENST00000395912.6:c.49-6015A>T	ENSP00000379248.2:n.49-6015A>T
ENST00000517517.1:n.513+100A>T
ENST00000519317.5:c.48+6778A>T	ENSP00000430641.1:n.48+6778A>T
ENST00000519962.5:c.48+6778A>T	ENSP00000429140.1:n.48+6778A>T
ENST00000522368.5:c.373+100A>T
ENST00000522394.1:c.122+182A>T	ENSP00000429578.1:n.122+182A>T
ENST00000523957.1:c.*127+100A>T	ENSP00000427830.1:n.*127+100A>T
ENST00000621845.1:c.42+100A>T	ENSP00000484318.1:n.42+100A>T
NM_001172477.1:c.420+100A>T , LRG_788t1:c.420+100A>T	NP_001165948.1:n.420+100A>T
NM_001172478.1:c.49-6015A>T	NP_001165949.1:n.49-6015A>T
NM_015713.4:c.204+100A>T , LRG_788t2:c.204+100A>T	NP_056528.2:n.204+100A>T
NM_001172478.2:c.49-6015A>T	NP_001165949.1:n.49-6015A>T
NM_015713.5:c.204+100A>T MANE Select	NP_056528.2:n.204+100A>T