Canonical Allele Identifier: CA1806674690

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208256A= , CM000670.2:g.102208256A=	GRCh38
NC_000008.10:g.103220484A= , CM000670.1:g.103220484A=	GRCh37
NC_000008.9:g.103289660A=	NCBI36
NG_016617.1:g.35863T= , LRG_788:g.35863T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.933T= MANE Select	ENSP00000251810.3:p.Phe311=
ENST00000251810.7:c.933T=	ENSP00000251810.3:p.Phe311=
ENST00000395910.6:n.320T=
ENST00000395912.6:c.777T=	ENSP00000379248.2:p.Phe259=
ENST00000519317.5:c.297T=	ENSP00000430641.1:p.Phe99=
ENST00000519962.5:c.78T=	ENSP00000429140.1:p.Phe26=
ENST00000522368.5:c.1102T=
ENST00000522394.1:c.266T=	ENSP00000429578.1:n.266T=
ENST00000621845.1:c.771T=	ENSP00000484318.1:p.Phe257=
NM_001172477.1:c.1149T= , LRG_788t1:c.1149T=	NP_001165948.1:p.Phe383=
NM_001172478.1:c.777T=	NP_001165949.1:p.Phe259=
NM_015713.4:c.933T= , LRG_788t2:c.933T=	NP_056528.2:p.Phe311=
NM_001172478.2:c.777T=	NP_001165949.1:p.Phe259=
NM_015713.5:c.933T= MANE Select	NP_056528.2:p.Phe311=