Canonical Allele Identifier: CA1806674679

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208217A= , CM000670.2:g.102208217A=	GRCh38
NC_000008.10:g.103220445A= , CM000670.1:g.103220445A=	GRCh37
NC_000008.9:g.103289621A=	NCBI36
NG_016617.1:g.35902T= , LRG_788:g.35902T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.972T= MANE Select	ENSP00000251810.3:p.Phe324=
ENST00000251810.7:c.972T=	ENSP00000251810.3:p.Phe324=
ENST00000395910.6:n.359T=
ENST00000395912.6:c.816T=	ENSP00000379248.2:p.Phe272=
ENST00000519317.5:c.336T=	ENSP00000430641.1:p.Phe112=
ENST00000519962.5:c.117T=	ENSP00000429140.1:p.Phe39=
ENST00000522368.5:c.1141T=
ENST00000522394.1:c.305T=	ENSP00000429578.1:n.305T=
ENST00000621845.1:c.810T=	ENSP00000484318.1:p.Phe270=
NM_001172477.1:c.1188T= , LRG_788t1:c.1188T=	NP_001165948.1:p.Phe396=
NM_001172478.1:c.816T=	NP_001165949.1:p.Phe272=
NM_015713.4:c.972T= , LRG_788t2:c.972T=	NP_056528.2:p.Phe324=
NM_001172478.2:c.816T=	NP_001165949.1:p.Phe272=
NM_015713.5:c.972T= MANE Select	NP_056528.2:p.Phe324=