Canonical Allele Identifier: CA1806687906

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238874T= , CM000670.2:g.102238874T=	GRCh38
NC_000008.10:g.103251102T= , CM000670.1:g.103251102T=	GRCh37
NC_000008.9:g.103320278T=	NCBI36
NG_016617.1:g.5245A= , LRG_788:g.5245A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1A= MANE Select	ENSP00000251810.3:p.Met1=
ENST00000251810.7:c.1A=	ENSP00000251810.3:p.Met1=
ENST00000395912.6:c.1A=	ENSP00000379248.2:p.Met1=
ENST00000519317.5:c.1A=	ENSP00000430641.1:p.Met1=
ENST00000519962.5:c.1A=	ENSP00000429140.1:p.Met1=
ENST00000522394.1:c.1A=	ENSP00000429578.1:p.Met1=
ENST00000523957.1:c.1A=	ENSP00000427830.1:p.Met1=
NM_001172478.1:c.1A=	NP_001165949.1:p.Met1=
NM_015713.4:c.1A= , LRG_788t2:c.1A=	NP_056528.2:p.Met1=
NM_001172478.2:c.1A=	NP_001165949.1:p.Met1=
NM_015713.5:c.1A= MANE Select	NP_056528.2:p.Met1=