Canonical Allele Identifier: CA1806686210

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232195C= , CM000670.2:g.102232195C=	GRCh38
NC_000008.10:g.103244423C= , CM000670.1:g.103244423C=	GRCh37
NC_000008.9:g.103313599C=	NCBI36
NG_016617.1:g.11924G= , LRG_788:g.11924G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.158G= MANE Select	ENSP00000251810.3:p.Trp53=
ENST00000251810.7:c.158G=	ENSP00000251810.3:p.Trp53=
ENST00000395912.6:c.49-6161G=	ENSP00000379248.2:n.49-6161G=
ENST00000517517.1:n.467G=
ENST00000519317.5:c.48+6632G=	ENSP00000430641.1:n.48+6632G=
ENST00000519962.5:c.48+6632G=	ENSP00000429140.1:n.48+6632G=
ENST00000522368.5:c.327G=
ENST00000522394.1:c.122+36G=	ENSP00000429578.1:n.122+36G=
ENST00000523957.1:c.*81G=	ENSP00000427830.1:n.*81G=
ENST00000621845.1:c.-5G=	ENSP00000484318.1:n.-5G=
NM_001172477.1:c.374G= , LRG_788t1:c.374G=	NP_001165948.1:p.Trp125=
NM_001172478.1:c.49-6161G=	NP_001165949.1:n.49-6161G=
NM_015713.4:c.158G= , LRG_788t2:c.158G=	NP_056528.2:p.Trp53=
NM_001172478.2:c.49-6161G=	NP_001165949.1:n.49-6161G=
NM_015713.5:c.158G= MANE Select	NP_056528.2:p.Trp53=