Canonical Allele Identifier: CA1806687877

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238827C= , CM000670.2:g.102238827C=	GRCh38
NC_000008.10:g.103251055C= , CM000670.1:g.103251055C=	GRCh37
NC_000008.9:g.103320231C=	NCBI36
NG_016617.1:g.5292G= , LRG_788:g.5292G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.48G= MANE Select	NP_056528.2:p.Glu16=
ENST00000251810.8:c.48G= MANE Select	ENSP00000251810.3:p.Glu16=
NM_001172477.1:c.-5G= , LRG_788t1:c.-5G=	NP_001165948.1:n.-5G=
NM_001172478.1:c.48G=	NP_001165949.1:p.Glu16=
NM_001172478.2:c.48G=	NP_001165949.1:p.Glu16=
NM_015713.4:c.48G= , LRG_788t2:c.48G=	NP_056528.2:p.Glu16=
ENST00000251810.7:c.48G=	ENSP00000251810.3:p.Glu16=
ENST00000395912.6:c.48G=	ENSP00000379248.2:p.Glu16=
ENST00000519317.5:c.48G=	ENSP00000430641.1:p.Glu16=
ENST00000519962.5:c.48G=	ENSP00000429140.1:p.Glu16=
ENST00000522394.1:c.48G=	ENSP00000429578.1:p.Glu16=
ENST00000523957.1:c.48G=	ENSP00000427830.1:p.Glu16=