Canonical Allele Identifier: CA1806674629

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208057A= , CM000670.2:g.102208057A=	GRCh38
NC_000008.10:g.103220285A= , CM000670.1:g.103220285A=	GRCh37
NC_000008.9:g.103289461A=	NCBI36
NG_016617.1:g.36062T= , LRG_788:g.36062T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.*76T= MANE Select	ENSP00000251810.3:n.*76T=
ENST00000251810.7:c.*76T=	ENSP00000251810.3:n.*76T=
ENST00000395910.6:n.519T=
ENST00000522368.5:c.1301T=
ENST00000621845.1:c.*76T=	ENSP00000484318.1:n.*76T=
NM_001172477.1:c.*76T= , LRG_788t1:c.*76T=	NP_001165948.1:n.*76T=
NM_001172478.1:c.*76T=	NP_001165949.1:n.*76T=
NM_015713.4:c.*76T= , LRG_788t2:c.*76T=	NP_056528.2:n.*76T=
NM_001172478.2:c.*76T=	NP_001165949.1:n.*76T=
NM_015713.5:c.*76T= MANE Select	NP_056528.2:n.*76T=