Canonical Allele Identifier: CA1806681688

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225011C= , CM000670.2:g.102225011C=	GRCh38
NC_000008.10:g.103237239C= , CM000670.1:g.103237239C=	GRCh37
NC_000008.9:g.103306415C=	NCBI36
NG_016617.1:g.19108G= , LRG_788:g.19108G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.329G= MANE Select	NP_056528.2:p.Arg110=
ENST00000251810.8:c.329G= MANE Select	ENSP00000251810.3:p.Arg110=
NM_001172477.1:c.545G= , LRG_788t1:c.545G=	NP_001165948.1:p.Arg182=
NM_001172478.1:c.173G=	NP_001165949.1:p.Arg58=
NM_001172478.2:c.173G=	NP_001165949.1:p.Arg58=
NM_015713.4:c.329G= , LRG_788t2:c.329G=	NP_056528.2:p.Arg110=
ENST00000251810.7:c.329G=	ENSP00000251810.3:p.Arg110=
ENST00000395912.6:c.173G=	ENSP00000379248.2:p.Arg58=
ENST00000519317.5:c.49-10853G=	ENSP00000430641.1:n.49-10853G=
ENST00000519962.5:c.48+13816G=	ENSP00000429140.1:n.48+13816G=
ENST00000522368.5:c.498G=
ENST00000522394.1:c.122+7220G=	ENSP00000429578.1:n.122+7220G=
ENST00000523957.1:c.*252G=	ENSP00000427830.1:n.*252G=
ENST00000621845.1:c.167G=	ENSP00000484318.1:p.Arg56=