Canonical Allele Identifier: CA844774639

Gene: RRM2B

Linked Data

• dbSNP Id: rs1165721663
• gnomAD v3: 8-102231881-A-AG
• gnomAD v4: 8-102231881-A-AG
• MyVariant Identifiers: chr8:g.103244109_103244110insG (hg19) ; chr8:g.102231881_102231882insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231881_102231882insG , CM000670.2:g.102231881_102231882insG	GRCh38
NC_000008.10:g.103244109_103244110insG , CM000670.1:g.103244109_103244110insG	GRCh37
NC_000008.9:g.103313285_103313286insG	NCBI36
NG_016617.1:g.12237_12238insC , LRG_788:g.12237_12238insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+267_204+268insC MANE Select	ENSP00000251810.3:n.204+267_204+268insC
ENST00000251810.7:c.204+267_204+268insC	ENSP00000251810.3:n.204+267_204+268insC
ENST00000395912.6:c.49-5848_49-5847insC	ENSP00000379248.2:n.49-5848_49-5847insC
ENST00000517517.1:n.513+267_513+268insC
ENST00000519317.5:c.48+6945_48+6946insC	ENSP00000430641.1:n.48+6945_48+6946insC
ENST00000519962.5:c.48+6945_48+6946insC	ENSP00000429140.1:n.48+6945_48+6946insC
ENST00000522368.5:c.373+267_373+268insC
ENST00000522394.1:c.122+349_122+350insC	ENSP00000429578.1:n.122+349_122+350insC
ENST00000523957.1:c.*127+267_*127+268insC	ENSP00000427830.1:n.*127+267_*127+268insC
ENST00000621845.1:c.42+267_42+268insC	ENSP00000484318.1:n.42+267_42+268insC
NM_001172477.1:c.420+267_420+268insC , LRG_788t1:c.420+267_420+268insC	NP_001165948.1:n.420+267_420+268insC
NM_001172478.1:c.49-5848_49-5847insC	NP_001165949.1:n.49-5848_49-5847insC
NM_015713.4:c.204+267_204+268insC , LRG_788t2:c.204+267_204+268insC	NP_056528.2:n.204+267_204+268insC
NM_001172478.2:c.49-5848_49-5847insC	NP_001165949.1:n.49-5848_49-5847insC
NM_015713.5:c.204+267_204+268insC MANE Select	NP_056528.2:n.204+267_204+268insC