Canonical Allele Identifier: CA371585257

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220384A>T (hg19) ; chr8:g.102208156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208156A>T , CM000670.2:g.102208156A>T	GRCh38
NC_000008.10:g.103220384A>T , CM000670.1:g.103220384A>T	GRCh37
NC_000008.9:g.103289560A>T	NCBI36
NG_016617.1:g.35963T>A , LRG_788:g.35963T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1033T>A MANE Select	ENSP00000251810.3:p.Phe345Ile
ENST00000251810.7:c.1033T>A	ENSP00000251810.3:p.Phe345Ile
ENST00000395910.6:n.420T>A
ENST00000395912.6:c.877T>A	ENSP00000379248.2:p.Phe293Ile
ENST00000519317.5:c.397T>A	ENSP00000430641.1:p.Phe133Ile
ENST00000519962.5:c.178T>A	ENSP00000429140.1:p.Phe60Ile
ENST00000522368.5:c.1202T>A
ENST00000522394.1:c.366T>A	ENSP00000429578.1:n.366T>A
ENST00000621845.1:c.871T>A	ENSP00000484318.1:p.Phe291Ile
NM_001172477.1:c.1249T>A , LRG_788t1:c.1249T>A	NP_001165948.1:p.Phe417Ile
NM_001172478.1:c.877T>A	NP_001165949.1:p.Phe293Ile
NM_015713.4:c.1033T>A , LRG_788t2:c.1033T>A	NP_056528.2:p.Phe345Ile
NM_001172478.2:c.877T>A	NP_001165949.1:p.Phe293Ile
NM_015713.5:c.1033T>A MANE Select	NP_056528.2:p.Phe345Ile