Canonical Allele Identifier: CA1806686204

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232182T= , CM000670.2:g.102232182T=	GRCh38
NC_000008.10:g.103244410T= , CM000670.1:g.103244410T=	GRCh37
NC_000008.9:g.103313586T=	NCBI36
NG_016617.1:g.11937A= , LRG_788:g.11937A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.171A= MANE Select	ENSP00000251810.3:p.Lys57=
ENST00000251810.7:c.171A=	ENSP00000251810.3:p.Lys57=
ENST00000395912.6:c.49-6148A=	ENSP00000379248.2:n.49-6148A=
ENST00000517517.1:n.480A=
ENST00000519317.5:c.48+6645A=	ENSP00000430641.1:n.48+6645A=
ENST00000519962.5:c.48+6645A=	ENSP00000429140.1:n.48+6645A=
ENST00000522368.5:c.340A=
ENST00000522394.1:c.122+49A=	ENSP00000429578.1:n.122+49A=
ENST00000523957.1:c.*94A=	ENSP00000427830.1:n.*94A=
ENST00000621845.1:c.9A=	ENSP00000484318.1:p.Lys3=
NM_001172477.1:c.387A= , LRG_788t1:c.387A=	NP_001165948.1:p.Lys129=
NM_001172478.1:c.49-6148A=	NP_001165949.1:n.49-6148A=
NM_015713.4:c.171A= , LRG_788t2:c.171A=	NP_056528.2:p.Lys57=
NM_001172478.2:c.49-6148A=	NP_001165949.1:n.49-6148A=
NM_015713.5:c.171A= MANE Select	NP_056528.2:p.Lys57=