Canonical Allele Identifier: CA462123648

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220361T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208133T>C , CM000670.2:g.102208133T>C	GRCh38
NC_000008.10:g.103220361T>C , CM000670.1:g.103220361T>C	GRCh37
NC_000008.9:g.103289537T>C	NCBI36
NG_016617.1:g.35986A>G , LRG_788:g.35986A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.1056A>G MANE Select	ENSP00000251810.3:p.Ter352=
ENST00000251810.7:c.1056A>G	ENSP00000251810.3:p.Ter352=
ENST00000395910.6:n.443A>G
ENST00000395912.6:c.900A>G	ENSP00000379248.2:p.Ter300=
ENST00000519317.5:c.420A>G	ENSP00000430641.1:p.Ter140=
ENST00000519962.5:c.201A>G	ENSP00000429140.1:p.Ter67=
ENST00000522368.5:c.1225A>G
ENST00000522394.1:c.389A>G	ENSP00000429578.1:n.389A>G
ENST00000621845.1:c.894A>G	ENSP00000484318.1:p.Ter298=
NM_001172477.1:c.1272A>G , LRG_788t1:c.1272A>G	NP_001165948.1:p.Ter424=
NM_001172478.1:c.900A>G	NP_001165949.1:p.Ter300=
NM_015713.4:c.1056A>G , LRG_788t2:c.1056A>G	NP_056528.2:p.Ter352=
NM_001172478.2:c.900A>G	NP_001165949.1:p.Ter300=
NM_015713.5:c.1056A>G MANE Select	NP_056528.2:p.Ter352=