Canonical Allele Identifier: CA1806687947

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238947C= , CM000670.2:g.102238947C=	GRCh38
NC_000008.10:g.103251175C= , CM000670.1:g.103251175C=	GRCh37
NC_000008.9:g.103320351C=	NCBI36
NG_016617.1:g.5172G= , LRG_788:g.5172G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.-73G= MANE Select	ENSP00000251810.3:n.-73G=
ENST00000251810.7:c.-73G=	ENSP00000251810.3:n.-73G=
NM_001172478.1:c.-73G=	NP_001165949.1:n.-73G=
NM_015713.4:c.-73G= , LRG_788t2:c.-73G=	NP_056528.2:n.-73G=
NM_001172478.2:c.-73G=	NP_001165949.1:n.-73G=
NM_015713.5:c.-73G= MANE Select	NP_056528.2:n.-73G=