Canonical Allele Identifier: CA1806674599

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102207961T= , CM000670.2:g.102207961T=	GRCh38
NC_000008.10:g.103220189T= , CM000670.1:g.103220189T=	GRCh37
NC_000008.9:g.103289365T=	NCBI36
NG_016617.1:g.36158A= , LRG_788:g.36158A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*172A= MANE Select	ENSP00000251810.3:n.*172A=
ENST00000251810.7:c.*172A=	ENSP00000251810.3:n.*172A=
ENST00000395910.6:n.615A=
ENST00000522368.5:c.1397A=
ENST00000621845.1:c.*172A=	ENSP00000484318.1:n.*172A=
NM_001172477.1:c.*172A= , LRG_788t1:c.*172A=	NP_001165948.1:n.*172A=
NM_001172478.1:c.*172A=	NP_001165949.1:n.*172A=
NM_015713.4:c.*172A= , LRG_788t2:c.*172A=	NP_056528.2:n.*172A=
NM_001172478.2:c.*172A=	NP_001165949.1:n.*172A=
NM_015713.5:c.*172A= MANE Select	NP_056528.2:n.*172A=