Canonical Allele Identifier: CA1806678438

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102218957A= , CM000670.2:g.102218957A=	GRCh38
NC_000008.10:g.103231185A= , CM000670.1:g.103231185A=	GRCh37
NC_000008.9:g.103300361A=	NCBI36
NG_016617.1:g.25162T= , LRG_788:g.25162T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.551-10T= MANE Select	ENSP00000251810.3:n.551-10T=
ENST00000251810.7:c.551-10T=	ENSP00000251810.3:n.551-10T=
ENST00000395912.6:c.395-10T=	ENSP00000379248.2:n.395-10T=
ENST00000519125.1:n.59T=
ENST00000519317.5:c.49-4799T=	ENSP00000430641.1:n.49-4799T=
ENST00000519962.5:c.49-10672T=	ENSP00000429140.1:n.49-10672T=
ENST00000522368.5:c.720-10T=
ENST00000522394.1:c.123-6068T=	ENSP00000429578.1:n.123-6068T=
ENST00000621845.1:c.389-10T=	ENSP00000484318.1:n.389-10T=
NM_001172477.1:c.767-10T= , LRG_788t1:c.767-10T=	NP_001165948.1:n.767-10T=
NM_001172478.1:c.395-10T=	NP_001165949.1:n.395-10T=
NM_015713.4:c.551-10T= , LRG_788t2:c.551-10T=	NP_056528.2:n.551-10T=
NM_001172478.2:c.395-10T=	NP_001165949.1:n.395-10T=
NM_015713.5:c.551-10T= MANE Select	NP_056528.2:n.551-10T=