Canonical Allele Identifier: CA1806677109

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102214157C= , CM000670.2:g.102214157C=	GRCh38
NC_000008.10:g.103226385C= , CM000670.1:g.103226385C=	GRCh37
NC_000008.9:g.103295561C=	NCBI36
NG_016617.1:g.29962G= , LRG_788:g.29962G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.686G= MANE Select	ENSP00000251810.3:p.Gly229=
ENST00000251810.7:c.686G=	ENSP00000251810.3:p.Gly229=
ENST00000395910.6:n.73G=
ENST00000395912.6:c.530G=	ENSP00000379248.2:p.Gly177=
ENST00000519125.1:n.204G=
ENST00000519317.5:c.50G=	ENSP00000430641.1:p.Gly17=
ENST00000519962.5:c.49-5872G=	ENSP00000429140.1:n.49-5872G=
ENST00000522368.5:c.855G=
ENST00000522394.1:c.123-1268G=	ENSP00000429578.1:n.123-1268G=
ENST00000621845.1:c.524G=	ENSP00000484318.1:p.Gly175=
NM_001172477.1:c.902G= , LRG_788t1:c.902G=	NP_001165948.1:p.Gly301=
NM_001172478.1:c.530G=	NP_001165949.1:p.Gly177=
NM_015713.4:c.686G= , LRG_788t2:c.686G=	NP_056528.2:p.Gly229=
NM_001172478.2:c.530G=	NP_001165949.1:p.Gly177=
NM_015713.5:c.686G= MANE Select	NP_056528.2:p.Gly229=