Canonical Allele Identifier: CA1806674659

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208128G= , CM000670.2:g.102208128G=	GRCh38
NC_000008.10:g.103220356G= , CM000670.1:g.103220356G=	GRCh37
NC_000008.9:g.103289532G=	NCBI36
NG_016617.1:g.35991C= , LRG_788:g.35991C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.*5C= MANE Select	ENSP00000251810.3:n.*5C=
ENST00000251810.7:c.*5C=	ENSP00000251810.3:n.*5C=
ENST00000395910.6:n.448C=
ENST00000522368.5:c.1230C=
ENST00000621845.1:c.*5C=	ENSP00000484318.1:n.*5C=
NM_001172477.1:c.*5C= , LRG_788t1:c.*5C=	NP_001165948.1:n.*5C=
NM_001172478.1:c.*5C=	NP_001165949.1:n.*5C=
NM_015713.4:c.*5C= , LRG_788t2:c.*5C=	NP_056528.2:n.*5C=
NM_001172478.2:c.*5C=	NP_001165949.1:n.*5C=
NM_015713.5:c.*5C= MANE Select	NP_056528.2:n.*5C=