Canonical Allele Identifier: CA371585177

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220365A>T (hg19) ; chr8:g.102208137A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208137A>T , CM000670.2:g.102208137A>T	GRCh38
NC_000008.10:g.103220365A>T , CM000670.1:g.103220365A>T	GRCh37
NC_000008.9:g.103289541A>T	NCBI36
NG_016617.1:g.35982T>A , LRG_788:g.35982T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1052T>A MANE Select	ENSP00000251810.3:p.Phe351Tyr
ENST00000251810.7:c.1052T>A	ENSP00000251810.3:p.Phe351Tyr
ENST00000395910.6:n.439T>A
ENST00000395912.6:c.896T>A	ENSP00000379248.2:p.Phe299Tyr
ENST00000519317.5:c.416T>A	ENSP00000430641.1:p.Phe139Tyr
ENST00000519962.5:c.197T>A	ENSP00000429140.1:p.Phe66Tyr
ENST00000522368.5:c.1221T>A
ENST00000522394.1:c.385T>A	ENSP00000429578.1:n.385T>A
ENST00000621845.1:c.890T>A	ENSP00000484318.1:p.Phe297Tyr
NM_001172477.1:c.1268T>A , LRG_788t1:c.1268T>A	NP_001165948.1:p.Phe423Tyr
NM_001172478.1:c.896T>A	NP_001165949.1:p.Phe299Tyr
NM_015713.4:c.1052T>A , LRG_788t2:c.1052T>A	NP_056528.2:p.Phe351Tyr
NM_001172478.2:c.896T>A	NP_001165949.1:p.Phe299Tyr
NM_015713.5:c.1052T>A MANE Select	NP_056528.2:p.Phe351Tyr