Canonical Allele Identifier: CA1806681689

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225012G= , CM000670.2:g.102225012G=	GRCh38
NC_000008.10:g.103237240G= , CM000670.1:g.103237240G=	GRCh37
NC_000008.9:g.103306416G=	NCBI36
NG_016617.1:g.19107C= , LRG_788:g.19107C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.328C= MANE Select	ENSP00000251810.3:p.Arg110=
ENST00000251810.7:c.328C=	ENSP00000251810.3:p.Arg110=
ENST00000395912.6:c.172C=	ENSP00000379248.2:p.Arg58=
ENST00000519317.5:c.49-10854C=	ENSP00000430641.1:n.49-10854C=
ENST00000519962.5:c.48+13815C=	ENSP00000429140.1:n.48+13815C=
ENST00000522368.5:c.497C=
ENST00000522394.1:c.122+7219C=	ENSP00000429578.1:n.122+7219C=
ENST00000523957.1:c.*251C=	ENSP00000427830.1:n.*251C=
ENST00000621845.1:c.166C=	ENSP00000484318.1:p.Arg56=
NM_001172477.1:c.544C= , LRG_788t1:c.544C=	NP_001165948.1:p.Arg182=
NM_001172478.1:c.172C=	NP_001165949.1:p.Arg58=
NM_015713.4:c.328C= , LRG_788t2:c.328C=	NP_056528.2:p.Arg110=
NM_001172478.2:c.172C=	NP_001165949.1:p.Arg58=
NM_015713.5:c.328C= MANE Select	NP_056528.2:p.Arg110=