Canonical Allele Identifier: CA371585184

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220368T>A (hg19) ; chr8:g.102208140T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208140T>A , CM000670.2:g.102208140T>A	GRCh38
NC_000008.10:g.103220368T>A , CM000670.1:g.103220368T>A	GRCh37
NC_000008.9:g.103289544T>A	NCBI36
NG_016617.1:g.35979A>T , LRG_788:g.35979A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1049A>T MANE Select	ENSP00000251810.3:p.Asp350Val
ENST00000251810.7:c.1049A>T	ENSP00000251810.3:p.Asp350Val
ENST00000395910.6:n.436A>T
ENST00000395912.6:c.893A>T	ENSP00000379248.2:p.Asp298Val
ENST00000519317.5:c.413A>T	ENSP00000430641.1:p.Asp138Val
ENST00000519962.5:c.194A>T	ENSP00000429140.1:p.Asp65Val
ENST00000522368.5:c.1218A>T
ENST00000522394.1:c.382A>T	ENSP00000429578.1:n.382A>T
ENST00000621845.1:c.887A>T	ENSP00000484318.1:p.Asp296Val
NM_001172477.1:c.1265A>T , LRG_788t1:c.1265A>T	NP_001165948.1:p.Asp422Val
NM_001172478.1:c.893A>T	NP_001165949.1:p.Asp298Val
NM_015713.4:c.1049A>T , LRG_788t2:c.1049A>T	NP_056528.2:p.Asp350Val
NM_001172478.2:c.893A>T	NP_001165949.1:p.Asp298Val
NM_015713.5:c.1049A>T MANE Select	NP_056528.2:p.Asp350Val