Canonical Allele Identifier: CA1806674688

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208243A= , CM000670.2:g.102208243A=	GRCh38
NC_000008.10:g.103220471A= , CM000670.1:g.103220471A=	GRCh37
NC_000008.9:g.103289647A=	NCBI36
NG_016617.1:g.35876T= , LRG_788:g.35876T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.946T= MANE Select	ENSP00000251810.3:p.Ser316=
ENST00000251810.7:c.946T=	ENSP00000251810.3:p.Ser316=
ENST00000395910.6:n.333T=
ENST00000395912.6:c.790T=	ENSP00000379248.2:p.Ser264=
ENST00000519317.5:c.310T=	ENSP00000430641.1:p.Ser104=
ENST00000519962.5:c.91T=	ENSP00000429140.1:p.Ser31=
ENST00000522368.5:c.1115T=
ENST00000522394.1:c.279T=	ENSP00000429578.1:n.279T=
ENST00000621845.1:c.784T=	ENSP00000484318.1:p.Ser262=
NM_001172477.1:c.1162T= , LRG_788t1:c.1162T=	NP_001165948.1:p.Ser388=
NM_001172478.1:c.790T=	NP_001165949.1:p.Ser264=
NM_015713.4:c.946T= , LRG_788t2:c.946T=	NP_056528.2:p.Ser316=
NM_001172478.2:c.790T=	NP_001165949.1:p.Ser264=
NM_015713.5:c.946T= MANE Select	NP_056528.2:p.Ser316=