Canonical Allele Identifier: CA918329686

Gene: RRM2B

Linked Data

• dbSNP Id: rs1554613342

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102238952_102238953insGTCCGC , CM000670.2:g.102238952_102238953insGTCCGC	GRCh38
NC_000008.10:g.103251180_103251181insGTCCGC , CM000670.1:g.103251180_103251181insGTCCGC	GRCh37
NC_000008.9:g.103320356_103320357insGTCCGC	NCBI36
NG_016617.1:g.5166_5167insGCGGAC , LRG_788:g.5166_5167insGCGGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000251810.8:c.-79_-78insGCGGAC MANE Select	ENSP00000251810.3:n.-79_-78insGCGGAC
ENST00000251810.7:c.-79_-78insGCGGAC	ENSP00000251810.3:n.-79_-78insGCGGAC
NM_001172478.1:c.-79_-78insGCGGAC	NP_001165949.1:n.-79_-78insGCGGAC
NM_015713.4:c.-79_-78insGCGGAC , LRG_788t2:c.-79_-78insGCGGAC	NP_056528.2:n.-79_-78insGCGGAC
NM_001172478.2:c.-79_-78insGCGGAC	NP_001165949.1:n.-79_-78insGCGGAC
NM_015713.5:c.-79_-78insGCGGAC MANE Select	NP_056528.2:n.-79_-78insGCGGAC