Canonical Allele Identifier: CA462123756

Gene: RRM2B

Linked Data

• dbSNP Id: rs1299858324
• MyVariant Identifiers: chr8:g.103220430T>G (hg19) ; chr8:g.102208202T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208202T>G , CM000670.2:g.102208202T>G	GRCh38
NC_000008.10:g.103220430T>G , CM000670.1:g.103220430T>G	GRCh37
NC_000008.9:g.103289606T>G	NCBI36
NG_016617.1:g.35917A>C , LRG_788:g.35917A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.987A>C MANE Select	ENSP00000251810.3:p.Ser329=
ENST00000251810.7:c.987A>C	ENSP00000251810.3:p.Ser329=
ENST00000395910.6:n.374A>C
ENST00000395912.6:c.831A>C	ENSP00000379248.2:p.Ser277=
ENST00000519317.5:c.351A>C	ENSP00000430641.1:p.Ser117=
ENST00000519962.5:c.132A>C	ENSP00000429140.1:p.Ser44=
ENST00000522368.5:c.1156A>C
ENST00000522394.1:c.320A>C	ENSP00000429578.1:n.320A>C
ENST00000621845.1:c.825A>C	ENSP00000484318.1:p.Ser275=
NM_001172477.1:c.1203A>C , LRG_788t1:c.1203A>C	NP_001165948.1:p.Ser401=
NM_001172478.1:c.831A>C	NP_001165949.1:p.Ser277=
NM_015713.4:c.987A>C , LRG_788t2:c.987A>C	NP_056528.2:p.Ser329=
NM_001172478.2:c.831A>C	NP_001165949.1:p.Ser277=
NM_015713.5:c.987A>C MANE Select	NP_056528.2:p.Ser329=