Canonical Allele Identifier: CA371585781

Gene: RRM2B

Linked Data

• MyVariant Identifiers: chr8:g.103220437C>A (hg19) ; chr8:g.102208209C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208209C>A , CM000670.2:g.102208209C>A	GRCh38
NC_000008.10:g.103220437C>A , CM000670.1:g.103220437C>A	GRCh37
NC_000008.9:g.103289613C>A	NCBI36
NG_016617.1:g.35910G>T , LRG_788:g.35910G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.980G>T MANE Select	ENSP00000251810.3:p.Arg327Leu
ENST00000251810.7:c.980G>T	ENSP00000251810.3:p.Arg327Leu
ENST00000395910.6:n.367G>T
ENST00000395912.6:c.824G>T	ENSP00000379248.2:p.Arg275Leu
ENST00000519317.5:c.344G>T	ENSP00000430641.1:p.Arg115Leu
ENST00000519962.5:c.125G>T	ENSP00000429140.1:p.Arg42Leu
ENST00000522368.5:c.1149G>T
ENST00000522394.1:c.313G>T	ENSP00000429578.1:n.313G>T
ENST00000621845.1:c.818G>T	ENSP00000484318.1:p.Arg273Leu
NM_001172477.1:c.1196G>T , LRG_788t1:c.1196G>T	NP_001165948.1:p.Arg399Leu
NM_001172478.1:c.824G>T	NP_001165949.1:p.Arg275Leu
NM_015713.4:c.980G>T , LRG_788t2:c.980G>T	NP_056528.2:p.Arg327Leu
NM_001172478.2:c.824G>T	NP_001165949.1:p.Arg275Leu
NM_015713.5:c.980G>T MANE Select	NP_056528.2:p.Arg327Leu