Canonical Allele Identifier: CA371585244

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220382G>C (hg19) ; chr8:g.102208154G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208154G>C , CM000670.2:g.102208154G>C	GRCh38
NC_000008.10:g.103220382G>C , CM000670.1:g.103220382G>C	GRCh37
NC_000008.9:g.103289558G>C	NCBI36
NG_016617.1:g.35965C>G , LRG_788:g.35965C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1035C>G MANE Select	ENSP00000251810.3:p.Phe345Leu
ENST00000251810.7:c.1035C>G	ENSP00000251810.3:p.Phe345Leu
ENST00000395910.6:n.422C>G
ENST00000395912.6:c.879C>G	ENSP00000379248.2:p.Phe293Leu
ENST00000519317.5:c.399C>G	ENSP00000430641.1:p.Phe133Leu
ENST00000519962.5:c.180C>G	ENSP00000429140.1:p.Phe60Leu
ENST00000522368.5:c.1204C>G
ENST00000522394.1:c.368C>G	ENSP00000429578.1:n.368C>G
ENST00000621845.1:c.873C>G	ENSP00000484318.1:p.Phe291Leu
NM_001172477.1:c.1251C>G , LRG_788t1:c.1251C>G	NP_001165948.1:p.Phe417Leu
NM_001172478.1:c.879C>G	NP_001165949.1:p.Phe293Leu
NM_015713.4:c.1035C>G , LRG_788t2:c.1035C>G	NP_056528.2:p.Phe345Leu
NM_001172478.2:c.879C>G	NP_001165949.1:p.Phe293Leu
NM_015713.5:c.1035C>G MANE Select	NP_056528.2:p.Phe345Leu