Canonical Allele Identifier: CA1806674662

Gene: RRM2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208151G= , CM000670.2:g.102208151G=	GRCh38
NC_000008.10:g.103220379G= , CM000670.1:g.103220379G=	GRCh37
NC_000008.9:g.103289555G=	NCBI36
NG_016617.1:g.35968C= , LRG_788:g.35968C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1038C= MANE Select	ENSP00000251810.3:p.Thr346=
ENST00000251810.7:c.1038C=	ENSP00000251810.3:p.Thr346=
ENST00000395910.6:n.425C=
ENST00000395912.6:c.882C=	ENSP00000379248.2:p.Thr294=
ENST00000519317.5:c.402C=	ENSP00000430641.1:p.Thr134=
ENST00000519962.5:c.183C=	ENSP00000429140.1:p.Thr61=
ENST00000522368.5:c.1207C=
ENST00000522394.1:c.371C=	ENSP00000429578.1:n.371C=
ENST00000621845.1:c.876C=	ENSP00000484318.1:p.Thr292=
NM_001172477.1:c.1254C= , LRG_788t1:c.1254C=	NP_001165948.1:p.Thr418=
NM_001172478.1:c.882C=	NP_001165949.1:p.Thr294=
NM_015713.4:c.1038C= , LRG_788t2:c.1038C=	NP_056528.2:p.Thr346=
NM_001172478.2:c.882C=	NP_001165949.1:p.Thr294=
NM_015713.5:c.1038C= MANE Select	NP_056528.2:p.Thr346=