Canonical Allele Identifier: CA371593139

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237210C>T (hg19) ; chr8:g.102224982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224982C>T , CM000670.2:g.102224982C>T	GRCh38
NC_000008.10:g.103237210C>T , CM000670.1:g.103237210C>T	GRCh37
NC_000008.9:g.103306386C>T	NCBI36
NG_016617.1:g.19137G>A , LRG_788:g.19137G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.358G>A MANE Select	ENSP00000251810.3:p.Ala120Thr
ENST00000251810.7:c.358G>A	ENSP00000251810.3:p.Ala120Thr
ENST00000395912.6:c.202G>A	ENSP00000379248.2:p.Ala68Thr
ENST00000519317.5:c.49-10824G>A	ENSP00000430641.1:n.49-10824G>A
ENST00000519962.5:c.48+13845G>A	ENSP00000429140.1:n.48+13845G>A
ENST00000522368.5:c.527G>A
ENST00000522394.1:c.122+7249G>A	ENSP00000429578.1:n.122+7249G>A
ENST00000523957.1:c.*281G>A	ENSP00000427830.1:n.*281G>A
ENST00000621845.1:c.196G>A	ENSP00000484318.1:p.Ala66Thr
NM_001172477.1:c.574G>A , LRG_788t1:c.574G>A	NP_001165948.1:p.Ala192Thr
NM_001172478.1:c.202G>A	NP_001165949.1:p.Ala68Thr
NM_015713.4:c.358G>A , LRG_788t2:c.358G>A	NP_056528.2:p.Ala120Thr
NM_001172478.2:c.202G>A	NP_001165949.1:p.Ala68Thr
NM_015713.5:c.358G>A MANE Select	NP_056528.2:p.Ala120Thr