Canonical Allele Identifier: CA371585256

Gene: RRM2B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1033T>C MANE Select	ENSP00000251810.3:p.Phe345Leu
ENST00000251810.7:c.1033T>C	ENSP00000251810.3:p.Phe345Leu
ENST00000395910.6:n.420T>C
ENST00000395912.6:c.877T>C	ENSP00000379248.2:p.Phe293Leu
ENST00000519317.5:c.397T>C	ENSP00000430641.1:p.Phe133Leu
ENST00000519962.5:c.178T>C	ENSP00000429140.1:p.Phe60Leu
ENST00000522368.5:c.1202T>C
ENST00000522394.1:c.366T>C	ENSP00000429578.1:n.366T>C
ENST00000621845.1:c.871T>C	ENSP00000484318.1:p.Phe291Leu
NM_001172477.1:c.1249T>C , LRG_788t1:c.1249T>C	NP_001165948.1:p.Phe417Leu
NM_001172478.1:c.877T>C	NP_001165949.1:p.Phe293Leu
NM_015713.4:c.1033T>C , LRG_788t2:c.1033T>C	NP_056528.2:p.Phe345Leu
NM_001172478.2:c.877T>C	NP_001165949.1:p.Phe293Leu
NM_015713.5:c.1033T>C MANE Select	NP_056528.2:p.Phe345Leu