Canonical Allele Identifier: CA462123657

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220370T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208142T>C , CM000670.2:g.102208142T>C	GRCh38
NC_000008.10:g.103220370T>C , CM000670.1:g.103220370T>C	GRCh37
NC_000008.9:g.103289546T>C	NCBI36
NG_016617.1:g.35977A>G , LRG_788:g.35977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1047A>G MANE Select	ENSP00000251810.3:p.Ala349=
ENST00000251810.7:c.1047A>G	ENSP00000251810.3:p.Ala349=
ENST00000395910.6:n.434A>G
ENST00000395912.6:c.891A>G	ENSP00000379248.2:p.Ala297=
ENST00000519317.5:c.411A>G	ENSP00000430641.1:p.Ala137=
ENST00000519962.5:c.192A>G	ENSP00000429140.1:p.Ala64=
ENST00000522368.5:c.1216A>G
ENST00000522394.1:c.380A>G	ENSP00000429578.1:n.380A>G
ENST00000621845.1:c.885A>G	ENSP00000484318.1:p.Ala295=
NM_001172477.1:c.1263A>G , LRG_788t1:c.1263A>G	NP_001165948.1:p.Ala421=
NM_001172478.1:c.891A>G	NP_001165949.1:p.Ala297=
NM_015713.4:c.1047A>G , LRG_788t2:c.1047A>G	NP_056528.2:p.Ala349=
NM_001172478.2:c.891A>G	NP_001165949.1:p.Ala297=
NM_015713.5:c.1047A>G MANE Select	NP_056528.2:p.Ala349=