Canonical Allele Identifier: CA1806681732

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225109A= , CM000670.2:g.102225109A=	GRCh38
NC_000008.10:g.103237337A= , CM000670.1:g.103237337A=	GRCh37
NC_000008.9:g.103306513A=	NCBI36
NG_016617.1:g.19010T= , LRG_788:g.19010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.322-91T= MANE Select	ENSP00000251810.3:n.322-91T=
ENST00000251810.7:c.322-91T=	ENSP00000251810.3:n.322-91T=
ENST00000395912.6:c.166-91T=	ENSP00000379248.2:n.166-91T=
ENST00000519317.5:c.49-10951T=	ENSP00000430641.1:n.49-10951T=
ENST00000519962.5:c.48+13718T=	ENSP00000429140.1:n.48+13718T=
ENST00000522368.5:c.491-91T=
ENST00000522394.1:c.122+7122T=	ENSP00000429578.1:n.122+7122T=
ENST00000523957.1:c.*245-91T=	ENSP00000427830.1:n.*245-91T=
ENST00000621845.1:c.160-91T=	ENSP00000484318.1:n.160-91T=
NM_001172477.1:c.538-91T= , LRG_788t1:c.538-91T=	NP_001165948.1:n.538-91T=
NM_001172478.1:c.166-91T=	NP_001165949.1:n.166-91T=
NM_015713.4:c.322-91T= , LRG_788t2:c.322-91T=	NP_056528.2:n.322-91T=
NM_001172478.2:c.166-91T=	NP_001165949.1:n.166-91T=
NM_015713.5:c.322-91T= MANE Select	NP_056528.2:n.322-91T=