Canonical Allele Identifier: CA1806687950

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238949C= , CM000670.2:g.102238949C=	GRCh38
NC_000008.10:g.103251177C= , CM000670.1:g.103251177C=	GRCh37
NC_000008.9:g.103320353C=	NCBI36
NG_016617.1:g.5170G= , LRG_788:g.5170G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.-75G= MANE Select	ENSP00000251810.3:n.-75G=
ENST00000251810.7:c.-75G=	ENSP00000251810.3:n.-75G=
NM_001172478.1:c.-75G=	NP_001165949.1:n.-75G=
NM_015713.4:c.-75G= , LRG_788t2:c.-75G=	NP_056528.2:n.-75G=
NM_001172478.2:c.-75G=	NP_001165949.1:n.-75G=
NM_015713.5:c.-75G= MANE Select	NP_056528.2:n.-75G=