Canonical Allele Identifier: CA1806674680

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208218A= , CM000670.2:g.102208218A=	GRCh38
NC_000008.10:g.103220446A= , CM000670.1:g.103220446A=	GRCh37
NC_000008.9:g.103289622A=	NCBI36
NG_016617.1:g.35901T= , LRG_788:g.35901T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.971T= MANE Select	ENSP00000251810.3:p.Phe324=
ENST00000251810.7:c.971T=	ENSP00000251810.3:p.Phe324=
ENST00000395910.6:n.358T=
ENST00000395912.6:c.815T=	ENSP00000379248.2:p.Phe272=
ENST00000519317.5:c.335T=	ENSP00000430641.1:p.Phe112=
ENST00000519962.5:c.116T=	ENSP00000429140.1:p.Phe39=
ENST00000522368.5:c.1140T=
ENST00000522394.1:c.304T=	ENSP00000429578.1:n.304T=
ENST00000621845.1:c.809T=	ENSP00000484318.1:p.Phe270=
NM_001172477.1:c.1187T= , LRG_788t1:c.1187T=	NP_001165948.1:p.Phe396=
NM_001172478.1:c.815T=	NP_001165949.1:p.Phe272=
NM_015713.4:c.971T= , LRG_788t2:c.971T=	NP_056528.2:p.Phe324=
NM_001172478.2:c.815T=	NP_001165949.1:p.Phe272=
NM_015713.5:c.971T= MANE Select	NP_056528.2:p.Phe324=