Canonical Allele Identifier: CA2688147440

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102232048-ATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232054_102232056del , CM000670.2:g.102232054_102232056del	GRCh38
NC_000008.10:g.103244282_103244284del , CM000670.1:g.103244282_103244284del	GRCh37
NC_000008.9:g.103313458_103313460del	NCBI36
NG_016617.1:g.12068_12070del , LRG_788:g.12068_12070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+98_204+100del MANE Select	ENSP00000251810.3:n.204+98_204+100del
ENST00000251810.7:c.204+98_204+100del	ENSP00000251810.3:n.204+98_204+100del
ENST00000395912.6:c.49-6017_49-6015del	ENSP00000379248.2:n.49-6017_49-6015del
ENST00000517517.1:n.513+98_513+100del
ENST00000519317.5:c.48+6776_48+6778del	ENSP00000430641.1:n.48+6776_48+6778del
ENST00000519962.5:c.48+6776_48+6778del	ENSP00000429140.1:n.48+6776_48+6778del
ENST00000522368.5:c.373+98_373+100del
ENST00000522394.1:c.122+180_122+182del	ENSP00000429578.1:n.122+180_122+182del
ENST00000523957.1:c.*127+98_*127+100del	ENSP00000427830.1:n.*127+98_*127+100del
ENST00000621845.1:c.42+98_42+100del	ENSP00000484318.1:n.42+98_42+100del
NM_001172477.1:c.420+98_420+100del , LRG_788t1:c.420+98_420+100del	NP_001165948.1:n.420+98_420+100del
NM_001172478.1:c.49-6017_49-6015del	NP_001165949.1:n.49-6017_49-6015del
NM_015713.4:c.204+98_204+100del , LRG_788t2:c.204+98_204+100del	NP_056528.2:n.204+98_204+100del
NM_001172478.2:c.49-6017_49-6015del	NP_001165949.1:n.49-6017_49-6015del
NM_015713.5:c.204+98_204+100del MANE Select	NP_056528.2:n.204+98_204+100del