Canonical Allele Identifier: CA371585206

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220374T>A (hg19) ; chr8:g.102208146T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208146T>A , CM000670.2:g.102208146T>A	GRCh38
NC_000008.10:g.103220374T>A , CM000670.1:g.103220374T>A	GRCh37
NC_000008.9:g.103289550T>A	NCBI36
NG_016617.1:g.35973A>T , LRG_788:g.35973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1043A>T MANE Select	ENSP00000251810.3:p.Asp348Val
ENST00000251810.7:c.1043A>T	ENSP00000251810.3:p.Asp348Val
ENST00000395910.6:n.430A>T
ENST00000395912.6:c.887A>T	ENSP00000379248.2:p.Asp296Val
ENST00000519317.5:c.407A>T	ENSP00000430641.1:p.Asp136Val
ENST00000519962.5:c.188A>T	ENSP00000429140.1:p.Asp63Val
ENST00000522368.5:c.1212A>T
ENST00000522394.1:c.376A>T	ENSP00000429578.1:n.376A>T
ENST00000621845.1:c.881A>T	ENSP00000484318.1:p.Asp294Val
NM_001172477.1:c.1259A>T , LRG_788t1:c.1259A>T	NP_001165948.1:p.Asp420Val
NM_001172478.1:c.887A>T	NP_001165949.1:p.Asp296Val
NM_015713.4:c.1043A>T , LRG_788t2:c.1043A>T	NP_056528.2:p.Asp348Val
NM_001172478.2:c.887A>T	NP_001165949.1:p.Asp296Val
NM_015713.5:c.1043A>T MANE Select	NP_056528.2:p.Asp348Val