Canonical Allele Identifier: CA371586218

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220474T>A (hg19) ; chr8:g.102208246T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208246T>A , CM000670.2:g.102208246T>A	GRCh38
NC_000008.10:g.103220474T>A , CM000670.1:g.103220474T>A	GRCh37
NC_000008.9:g.103289650T>A	NCBI36
NG_016617.1:g.35873A>T , LRG_788:g.35873A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.943A>T MANE Select	ENSP00000251810.3:p.Ile315Phe
ENST00000251810.7:c.943A>T	ENSP00000251810.3:p.Ile315Phe
ENST00000395910.6:n.330A>T
ENST00000395912.6:c.787A>T	ENSP00000379248.2:p.Ile263Phe
ENST00000519317.5:c.307A>T	ENSP00000430641.1:p.Ile103Phe
ENST00000519962.5:c.88A>T	ENSP00000429140.1:p.Ile30Phe
ENST00000522368.5:c.1112A>T
ENST00000522394.1:c.276A>T	ENSP00000429578.1:n.276A>T
ENST00000621845.1:c.781A>T	ENSP00000484318.1:p.Ile261Phe
NM_001172477.1:c.1159A>T , LRG_788t1:c.1159A>T	NP_001165948.1:p.Ile387Phe
NM_001172478.1:c.787A>T	NP_001165949.1:p.Ile263Phe
NM_015713.4:c.943A>T , LRG_788t2:c.943A>T	NP_056528.2:p.Ile315Phe
NM_001172478.2:c.787A>T	NP_001165949.1:p.Ile263Phe
NM_015713.5:c.943A>T MANE Select	NP_056528.2:p.Ile315Phe