Canonical Allele Identifier: CA371586175

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220467A>G (hg19) ; chr8:g.102208239A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208239A>G , CM000670.2:g.102208239A>G	GRCh38
NC_000008.10:g.103220467A>G , CM000670.1:g.103220467A>G	GRCh37
NC_000008.9:g.103289643A>G	NCBI36
NG_016617.1:g.35880T>C , LRG_788:g.35880T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.950T>C MANE Select	ENSP00000251810.3:p.Leu317Ser
ENST00000251810.7:c.950T>C	ENSP00000251810.3:p.Leu317Ser
ENST00000395910.6:n.337T>C
ENST00000395912.6:c.794T>C	ENSP00000379248.2:p.Leu265Ser
ENST00000519317.5:c.314T>C	ENSP00000430641.1:p.Leu105Ser
ENST00000519962.5:c.95T>C	ENSP00000429140.1:p.Leu32Ser
ENST00000522368.5:c.1119T>C
ENST00000522394.1:c.283T>C	ENSP00000429578.1:n.283T>C
ENST00000621845.1:c.788T>C	ENSP00000484318.1:p.Leu263Ser
NM_001172477.1:c.1166T>C , LRG_788t1:c.1166T>C	NP_001165948.1:p.Leu389Ser
NM_001172478.1:c.794T>C	NP_001165949.1:p.Leu265Ser
NM_015713.4:c.950T>C , LRG_788t2:c.950T>C	NP_056528.2:p.Leu317Ser
NM_001172478.2:c.794T>C	NP_001165949.1:p.Leu265Ser
NM_015713.5:c.950T>C MANE Select	NP_056528.2:p.Leu317Ser