Canonical Allele Identifier: CA371585229

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220378A>C (hg19) ; chr8:g.102208150A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208150A>C , CM000670.2:g.102208150A>C	GRCh38
NC_000008.10:g.103220378A>C , CM000670.1:g.103220378A>C	GRCh37
NC_000008.9:g.103289554A>C	NCBI36
NG_016617.1:g.35969T>G , LRG_788:g.35969T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.1039T>G MANE Select	ENSP00000251810.3:p.Leu347Val
ENST00000251810.7:c.1039T>G	ENSP00000251810.3:p.Leu347Val
ENST00000395910.6:n.426T>G
ENST00000395912.6:c.883T>G	ENSP00000379248.2:p.Leu295Val
ENST00000519317.5:c.403T>G	ENSP00000430641.1:p.Leu135Val
ENST00000519962.5:c.184T>G	ENSP00000429140.1:p.Leu62Val
ENST00000522368.5:c.1208T>G
ENST00000522394.1:c.372T>G	ENSP00000429578.1:n.372T>G
ENST00000621845.1:c.877T>G	ENSP00000484318.1:p.Leu293Val
NM_001172477.1:c.1255T>G , LRG_788t1:c.1255T>G	NP_001165948.1:p.Leu419Val
NM_001172478.1:c.883T>G	NP_001165949.1:p.Leu295Val
NM_015713.4:c.1039T>G , LRG_788t2:c.1039T>G	NP_056528.2:p.Leu347Val
NM_001172478.2:c.883T>G	NP_001165949.1:p.Leu295Val
NM_015713.5:c.1039T>G MANE Select	NP_056528.2:p.Leu347Val