Canonical Allele Identifier: CA2688147173

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102225096-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102225097_102225098del , CM000670.2:g.102225097_102225098del	GRCh38
NC_000008.10:g.103237325_103237326del , CM000670.1:g.103237325_103237326del	GRCh37
NC_000008.9:g.103306501_103306502del	NCBI36
NG_016617.1:g.19021_19022del , LRG_788:g.19021_19022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.322-80_322-79del MANE Select	ENSP00000251810.3:n.322-80_322-79del
ENST00000251810.7:c.322-80_322-79del	ENSP00000251810.3:n.322-80_322-79del
ENST00000395912.6:c.166-80_166-79del	ENSP00000379248.2:n.166-80_166-79del
ENST00000519317.5:c.49-10940_49-10939del	ENSP00000430641.1:n.49-10940_49-10939del
ENST00000519962.5:c.48+13729_48+13730del	ENSP00000429140.1:n.48+13729_48+13730del
ENST00000522368.5:c.491-80_491-79del
ENST00000522394.1:c.122+7133_122+7134del	ENSP00000429578.1:n.122+7133_122+7134del
ENST00000523957.1:c.*245-80_*245-79del	ENSP00000427830.1:n.*245-80_*245-79del
ENST00000621845.1:c.160-80_160-79del	ENSP00000484318.1:n.160-80_160-79del
NM_001172477.1:c.538-80_538-79del , LRG_788t1:c.538-80_538-79del	NP_001165948.1:n.538-80_538-79del
NM_001172478.1:c.166-80_166-79del	NP_001165949.1:n.166-80_166-79del
NM_015713.4:c.322-80_322-79del , LRG_788t2:c.322-80_322-79del	NP_056528.2:n.322-80_322-79del
NM_001172478.2:c.166-80_166-79del	NP_001165949.1:n.166-80_166-79del
NM_015713.5:c.322-80_322-79del MANE Select	NP_056528.2:n.322-80_322-79del