Canonical Allele Identifier: CA371585192

Gene: RRM2B

Linked Data

• COSMIC: COSM6256900
• MyVariant Identifiers: chr8:g.103220371G>T (hg19) ; chr8:g.102208143G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208143G>T , CM000670.2:g.102208143G>T	GRCh38
NC_000008.10:g.103220371G>T , CM000670.1:g.103220371G>T	GRCh37
NC_000008.9:g.103289547G>T	NCBI36
NG_016617.1:g.35976C>A , LRG_788:g.35976C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.1046C>A MANE Select	ENSP00000251810.3:p.Ala349Glu
ENST00000251810.7:c.1046C>A	ENSP00000251810.3:p.Ala349Glu
ENST00000395910.6:n.433C>A
ENST00000395912.6:c.890C>A	ENSP00000379248.2:p.Ala297Glu
ENST00000519317.5:c.410C>A	ENSP00000430641.1:p.Ala137Glu
ENST00000519962.5:c.191C>A	ENSP00000429140.1:p.Ala64Glu
ENST00000522368.5:c.1215C>A
ENST00000522394.1:c.379C>A	ENSP00000429578.1:n.379C>A
ENST00000621845.1:c.884C>A	ENSP00000484318.1:p.Ala295Glu
NM_001172477.1:c.1262C>A , LRG_788t1:c.1262C>A	NP_001165948.1:p.Ala421Glu
NM_001172478.1:c.890C>A	NP_001165949.1:p.Ala297Glu
NM_015713.4:c.1046C>A , LRG_788t2:c.1046C>A	NP_056528.2:p.Ala349Glu
NM_001172478.2:c.890C>A	NP_001165949.1:p.Ala297Glu
NM_015713.5:c.1046C>A MANE Select	NP_056528.2:p.Ala349Glu