Canonical Allele Identifier: CA371586055

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220455G>C (hg19) ; chr8:g.102208227G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208227G>C , CM000670.2:g.102208227G>C	GRCh38
NC_000008.10:g.103220455G>C , CM000670.1:g.103220455G>C	GRCh37
NC_000008.9:g.103289631G>C	NCBI36
NG_016617.1:g.35892C>G , LRG_788:g.35892C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.962C>G MANE Select	ENSP00000251810.3:p.Thr321Arg
ENST00000251810.7:c.962C>G	ENSP00000251810.3:p.Thr321Arg
ENST00000395910.6:n.349C>G
ENST00000395912.6:c.806C>G	ENSP00000379248.2:p.Thr269Arg
ENST00000519317.5:c.326C>G	ENSP00000430641.1:p.Thr109Arg
ENST00000519962.5:c.107C>G	ENSP00000429140.1:p.Thr36Arg
ENST00000522368.5:c.1131C>G
ENST00000522394.1:c.295C>G	ENSP00000429578.1:n.295C>G
ENST00000621845.1:c.800C>G	ENSP00000484318.1:p.Thr267Arg
NM_001172477.1:c.1178C>G , LRG_788t1:c.1178C>G	NP_001165948.1:p.Thr393Arg
NM_001172478.1:c.806C>G	NP_001165949.1:p.Thr269Arg
NM_015713.4:c.962C>G , LRG_788t2:c.962C>G	NP_056528.2:p.Thr321Arg
NM_001172478.2:c.806C>G	NP_001165949.1:p.Thr269Arg
NM_015713.5:c.962C>G MANE Select	NP_056528.2:p.Thr321Arg