Canonical Allele Identifier: CA2688147131

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102224850-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102224852dup , CM000670.2:g.102224852dup	GRCh38
NC_000008.10:g.103237080dup , CM000670.1:g.103237080dup	GRCh37
NC_000008.9:g.103306256dup	NCBI36
NG_016617.1:g.19268dup , LRG_788:g.19268dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.455+34dup MANE Select	ENSP00000251810.3:n.455+34dup
ENST00000251810.7:c.455+34dup	ENSP00000251810.3:n.455+34dup
ENST00000395912.6:c.299+34dup	ENSP00000379248.2:n.299+34dup
ENST00000519317.5:c.49-10693dup	ENSP00000430641.1:n.49-10693dup
ENST00000519962.5:c.48+13976dup	ENSP00000429140.1:n.48+13976dup
ENST00000522368.5:c.624+34dup
ENST00000522394.1:c.122+7380dup	ENSP00000429578.1:n.122+7380dup
ENST00000621845.1:c.293+34dup	ENSP00000484318.1:n.293+34dup
NM_001172477.1:c.671+34dup , LRG_788t1:c.671+34dup	NP_001165948.1:n.671+34dup
NM_001172478.1:c.299+34dup	NP_001165949.1:n.299+34dup
NM_015713.4:c.455+34dup , LRG_788t2:c.455+34dup	NP_056528.2:n.455+34dup
NM_001172478.2:c.299+34dup	NP_001165949.1:n.299+34dup
NM_015713.5:c.455+34dup MANE Select	NP_056528.2:n.455+34dup