Canonical Allele Identifier: CA462128439

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102232149-C-T
• MyVariant Identifiers: chr8:g.103244377C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232149C>T , CM000670.2:g.102232149C>T	GRCh38
NC_000008.10:g.103244377C>T , CM000670.1:g.103244377C>T	GRCh37
NC_000008.9:g.103313553C>T	NCBI36
NG_016617.1:g.11970G>A , LRG_788:g.11970G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.204G>A MANE Select	ENSP00000251810.3:p.Glu68=
ENST00000251810.7:c.204G>A	ENSP00000251810.3:p.Glu68=
ENST00000395912.6:c.49-6115G>A	ENSP00000379248.2:n.49-6115G>A
ENST00000517517.1:n.513G>A
ENST00000519317.5:c.48+6678G>A	ENSP00000430641.1:n.48+6678G>A
ENST00000519962.5:c.48+6678G>A	ENSP00000429140.1:n.48+6678G>A
ENST00000522368.5:c.373G>A
ENST00000522394.1:c.122+82G>A	ENSP00000429578.1:n.122+82G>A
ENST00000523957.1:c.*127G>A	ENSP00000427830.1:n.*127G>A
ENST00000621845.1:c.42G>A	ENSP00000484318.1:p.Glu14=
NM_001172477.1:c.420G>A , LRG_788t1:c.420G>A	NP_001165948.1:p.Glu140=
NM_001172478.1:c.49-6115G>A	NP_001165949.1:n.49-6115G>A
NM_015713.4:c.204G>A , LRG_788t2:c.204G>A	NP_056528.2:p.Glu68=
NM_001172478.2:c.49-6115G>A	NP_001165949.1:n.49-6115G>A
NM_015713.5:c.204G>A MANE Select	NP_056528.2:p.Glu68=