Canonical Allele Identifier: CA371585213

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220375C>T (hg19) ; chr8:g.102208147C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208147C>T , CM000670.2:g.102208147C>T	GRCh38
NC_000008.10:g.103220375C>T , CM000670.1:g.103220375C>T	GRCh37
NC_000008.9:g.103289551C>T	NCBI36
NG_016617.1:g.35972G>A , LRG_788:g.35972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1042G>A MANE Select	ENSP00000251810.3:p.Asp348Asn
ENST00000251810.7:c.1042G>A	ENSP00000251810.3:p.Asp348Asn
ENST00000395910.6:n.429G>A
ENST00000395912.6:c.886G>A	ENSP00000379248.2:p.Asp296Asn
ENST00000519317.5:c.406G>A	ENSP00000430641.1:p.Asp136Asn
ENST00000519962.5:c.187G>A	ENSP00000429140.1:p.Asp63Asn
ENST00000522368.5:c.1211G>A
ENST00000522394.1:c.375G>A	ENSP00000429578.1:n.375G>A
ENST00000621845.1:c.880G>A	ENSP00000484318.1:p.Asp294Asn
NM_001172477.1:c.1258G>A , LRG_788t1:c.1258G>A	NP_001165948.1:p.Asp420Asn
NM_001172478.1:c.886G>A	NP_001165949.1:p.Asp296Asn
NM_015713.4:c.1042G>A , LRG_788t2:c.1042G>A	NP_056528.2:p.Asp348Asn
NM_001172478.2:c.886G>A	NP_001165949.1:p.Asp296Asn
NM_015713.5:c.1042G>A MANE Select	NP_056528.2:p.Asp348Asn