Canonical Allele Identifier: CA371585902

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220444C>T (hg19) ; chr8:g.102208216C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208216C>T , CM000670.2:g.102208216C>T	GRCh38
NC_000008.10:g.103220444C>T , CM000670.1:g.103220444C>T	GRCh37
NC_000008.9:g.103289620C>T	NCBI36
NG_016617.1:g.35903G>A , LRG_788:g.35903G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.973G>A MANE Select	ENSP00000251810.3:p.Glu325Lys
ENST00000251810.7:c.973G>A	ENSP00000251810.3:p.Glu325Lys
ENST00000395910.6:n.360G>A
ENST00000395912.6:c.817G>A	ENSP00000379248.2:p.Glu273Lys
ENST00000519317.5:c.337G>A	ENSP00000430641.1:p.Glu113Lys
ENST00000519962.5:c.118G>A	ENSP00000429140.1:p.Glu40Lys
ENST00000522368.5:c.1142G>A
ENST00000522394.1:c.306G>A	ENSP00000429578.1:n.306G>A
ENST00000621845.1:c.811G>A	ENSP00000484318.1:p.Glu271Lys
NM_001172477.1:c.1189G>A , LRG_788t1:c.1189G>A	NP_001165948.1:p.Glu397Lys
NM_001172478.1:c.817G>A	NP_001165949.1:p.Glu273Lys
NM_015713.4:c.973G>A , LRG_788t2:c.973G>A	NP_056528.2:p.Glu325Lys
NM_001172478.2:c.817G>A	NP_001165949.1:p.Glu273Lys
NM_015713.5:c.973G>A MANE Select	NP_056528.2:p.Glu325Lys