Canonical Allele Identifier: CA371586065

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220456T>G (hg19) ; chr8:g.102208228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208228T>G , CM000670.2:g.102208228T>G	GRCh38
NC_000008.10:g.103220456T>G , CM000670.1:g.103220456T>G	GRCh37
NC_000008.9:g.103289632T>G	NCBI36
NG_016617.1:g.35891A>C , LRG_788:g.35891A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.961A>C MANE Select	ENSP00000251810.3:p.Thr321Pro
ENST00000251810.7:c.961A>C	ENSP00000251810.3:p.Thr321Pro
ENST00000395910.6:n.348A>C
ENST00000395912.6:c.805A>C	ENSP00000379248.2:p.Thr269Pro
ENST00000519317.5:c.325A>C	ENSP00000430641.1:p.Thr109Pro
ENST00000519962.5:c.106A>C	ENSP00000429140.1:p.Thr36Pro
ENST00000522368.5:c.1130A>C
ENST00000522394.1:c.294A>C	ENSP00000429578.1:n.294A>C
ENST00000621845.1:c.799A>C	ENSP00000484318.1:p.Thr267Pro
NM_001172477.1:c.1177A>C , LRG_788t1:c.1177A>C	NP_001165948.1:p.Thr393Pro
NM_001172478.1:c.805A>C	NP_001165949.1:p.Thr269Pro
NM_015713.4:c.961A>C , LRG_788t2:c.961A>C	NP_056528.2:p.Thr321Pro
NM_001172478.2:c.805A>C	NP_001165949.1:p.Thr269Pro
NM_015713.5:c.961A>C MANE Select	NP_056528.2:p.Thr321Pro