Canonical Allele Identifier: CA4831009

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102214088C>T , CM000670.2:g.102214088C>T	GRCh38
NC_000008.10:g.103226316C>T , CM000670.1:g.103226316C>T	GRCh37
NC_000008.9:g.103295492C>T	NCBI36
NG_016617.1:g.30031G>A , LRG_788:g.30031G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.755G>A MANE Select	NP_056528.2:p.Arg252Lys
ENST00000251810.8:c.755G>A MANE Select	ENSP00000251810.3:p.Arg252Lys
NM_001172477.1:c.971G>A , LRG_788t1:c.971G>A	NP_001165948.1:p.Arg324Lys
NM_001172478.1:c.599G>A	NP_001165949.1:p.Arg200Lys
NM_001172478.2:c.599G>A	NP_001165949.1:p.Arg200Lys
NM_015713.4:c.755G>A , LRG_788t2:c.755G>A	NP_056528.2:p.Arg252Lys
ENST00000251810.7:c.755G>A	ENSP00000251810.3:p.Arg252Lys
ENST00000395910.6:n.142G>A
ENST00000395912.6:c.599G>A	ENSP00000379248.2:p.Arg200Lys
ENST00000519125.1:n.273G>A
ENST00000519317.5:c.119G>A	ENSP00000430641.1:p.Arg40Lys
ENST00000519962.5:c.49-5803G>A	ENSP00000429140.1:n.49-5803G>A
ENST00000522368.5:c.924G>A
ENST00000522394.1:c.123-1199G>A	ENSP00000429578.1:n.123-1199G>A
ENST00000621845.1:c.593G>A	ENSP00000484318.1:p.Arg198Lys