Canonical Allele Identifier: CA371585190

Gene: RRM2B

Linked Data

• COSMIC: COSM3884206
• MyVariant Identifiers: chr8:g.103220371G>A (hg19) ; chr8:g.102208143G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1046C>T MANE Select	ENSP00000251810.3:p.Ala349Val
ENST00000251810.7:c.1046C>T	ENSP00000251810.3:p.Ala349Val
ENST00000395910.6:n.433C>T
ENST00000395912.6:c.890C>T	ENSP00000379248.2:p.Ala297Val
ENST00000519317.5:c.410C>T	ENSP00000430641.1:p.Ala137Val
ENST00000519962.5:c.191C>T	ENSP00000429140.1:p.Ala64Val
ENST00000522368.5:c.1215C>T
ENST00000522394.1:c.379C>T	ENSP00000429578.1:n.379C>T
ENST00000621845.1:c.884C>T	ENSP00000484318.1:p.Ala295Val
NM_001172477.1:c.1262C>T , LRG_788t1:c.1262C>T	NP_001165948.1:p.Ala421Val
NM_001172478.1:c.890C>T	NP_001165949.1:p.Ala297Val
NM_015713.4:c.1046C>T , LRG_788t2:c.1046C>T	NP_056528.2:p.Ala349Val
NM_001172478.2:c.890C>T	NP_001165949.1:p.Ala297Val
NM_015713.5:c.1046C>T MANE Select	NP_056528.2:p.Ala349Val