Canonical Allele Identifier: CA1806678315

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218899C= , CM000670.2:g.102218899C=	GRCh38
NC_000008.10:g.103231127C= , CM000670.1:g.103231127C=	GRCh37
NC_000008.9:g.103300303C=	NCBI36
NG_016617.1:g.25220G= , LRG_788:g.25220G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015713.5:c.599G= MANE Select	NP_056528.2:p.Gly200=
ENST00000251810.8:c.599G= MANE Select	ENSP00000251810.3:p.Gly200=
NM_001172477.1:c.815G= , LRG_788t1:c.815G=	NP_001165948.1:p.Gly272=
NM_001172478.1:c.443G=	NP_001165949.1:p.Gly148=
NM_001172478.2:c.443G=	NP_001165949.1:p.Gly148=
NM_015713.4:c.599G= , LRG_788t2:c.599G=	NP_056528.2:p.Gly200=
ENST00000251810.7:c.599G=	ENSP00000251810.3:p.Gly200=
ENST00000395912.6:c.443G=	ENSP00000379248.2:p.Gly148=
ENST00000519125.1:n.117G=
ENST00000519317.5:c.49-4741G=	ENSP00000430641.1:n.49-4741G=
ENST00000519962.5:c.49-10614G=	ENSP00000429140.1:n.49-10614G=
ENST00000522368.5:c.768G=
ENST00000522394.1:c.123-6010G=	ENSP00000429578.1:n.123-6010G=
ENST00000621845.1:c.437G=	ENSP00000484318.1:p.Gly146=