Canonical Allele Identifier: CA371592171

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103237113C>A (hg19) ; chr8:g.102224885C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224885C>A , CM000670.2:g.102224885C>A	GRCh38
NC_000008.10:g.103237113C>A , CM000670.1:g.103237113C>A	GRCh37
NC_000008.9:g.103306289C>A	NCBI36
NG_016617.1:g.19234G>T , LRG_788:g.19234G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.455G>T MANE Select	ENSP00000251810.3:p.Arg152Met
ENST00000251810.7:c.455G>T	ENSP00000251810.3:p.Arg152Met
ENST00000395912.6:c.299G>T	ENSP00000379248.2:p.Arg100Met
ENST00000519317.5:c.49-10727G>T	ENSP00000430641.1:n.49-10727G>T
ENST00000519962.5:c.48+13942G>T	ENSP00000429140.1:n.48+13942G>T
ENST00000522368.5:c.624G>T
ENST00000522394.1:c.122+7346G>T	ENSP00000429578.1:n.122+7346G>T
ENST00000621845.1:c.293G>T	ENSP00000484318.1:p.Arg98Met
NM_001172477.1:c.671G>T , LRG_788t1:c.671G>T	NP_001165948.1:p.Arg224Met
NM_001172478.1:c.299G>T	NP_001165949.1:p.Arg100Met
NM_015713.4:c.455G>T , LRG_788t2:c.455G>T	NP_056528.2:p.Arg152Met
NM_001172478.2:c.299G>T	NP_001165949.1:p.Arg100Met
NM_015713.5:c.455G>T MANE Select	NP_056528.2:p.Arg152Met