Canonical Allele Identifier: CA371586000

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220450A>C (hg19) ; chr8:g.102208222A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208222A>C , CM000670.2:g.102208222A>C	GRCh38
NC_000008.10:g.103220450A>C , CM000670.1:g.103220450A>C	GRCh37
NC_000008.9:g.103289626A>C	NCBI36
NG_016617.1:g.35897T>G , LRG_788:g.35897T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.967T>G MANE Select	ENSP00000251810.3:p.Phe323Val
ENST00000251810.7:c.967T>G	ENSP00000251810.3:p.Phe323Val
ENST00000395910.6:n.354T>G
ENST00000395912.6:c.811T>G	ENSP00000379248.2:p.Phe271Val
ENST00000519317.5:c.331T>G	ENSP00000430641.1:p.Phe111Val
ENST00000519962.5:c.112T>G	ENSP00000429140.1:p.Phe38Val
ENST00000522368.5:c.1136T>G
ENST00000522394.1:c.300T>G	ENSP00000429578.1:n.300T>G
ENST00000621845.1:c.805T>G	ENSP00000484318.1:p.Phe269Val
NM_001172477.1:c.1183T>G , LRG_788t1:c.1183T>G	NP_001165948.1:p.Phe395Val
NM_001172478.1:c.811T>G	NP_001165949.1:p.Phe271Val
NM_015713.4:c.967T>G , LRG_788t2:c.967T>G	NP_056528.2:p.Phe323Val
NM_001172478.2:c.811T>G	NP_001165949.1:p.Phe271Val
NM_015713.5:c.967T>G MANE Select	NP_056528.2:p.Phe323Val