Canonical Allele Identifier: CA1806681730

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225103C= , CM000670.2:g.102225103C=	GRCh38
NC_000008.10:g.103237331C= , CM000670.1:g.103237331C=	GRCh37
NC_000008.9:g.103306507C=	NCBI36
NG_016617.1:g.19016G= , LRG_788:g.19016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.322-85G= MANE Select	ENSP00000251810.3:n.322-85G=
ENST00000251810.7:c.322-85G=	ENSP00000251810.3:n.322-85G=
ENST00000395912.6:c.166-85G=	ENSP00000379248.2:n.166-85G=
ENST00000519317.5:c.49-10945G=	ENSP00000430641.1:n.49-10945G=
ENST00000519962.5:c.48+13724G=	ENSP00000429140.1:n.48+13724G=
ENST00000522368.5:c.491-85G=
ENST00000522394.1:c.122+7128G=	ENSP00000429578.1:n.122+7128G=
ENST00000523957.1:c.*245-85G=	ENSP00000427830.1:n.*245-85G=
ENST00000621845.1:c.160-85G=	ENSP00000484318.1:n.160-85G=
NM_001172477.1:c.538-85G= , LRG_788t1:c.538-85G=	NP_001165948.1:n.538-85G=
NM_001172478.1:c.166-85G=	NP_001165949.1:n.166-85G=
NM_015713.4:c.322-85G= , LRG_788t2:c.322-85G=	NP_056528.2:n.322-85G=
NM_001172478.2:c.166-85G=	NP_001165949.1:n.166-85G=
NM_015713.5:c.322-85G= MANE Select	NP_056528.2:n.322-85G=