Canonical Allele Identifier: CA2688143448

Gene: RRM2B

Linked Data

• gnomAD v4: 8-102208227-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102208232del , CM000670.2:g.102208232del	GRCh38
NC_000008.10:g.103220460del , CM000670.1:g.103220460del	GRCh37
NC_000008.9:g.103289636del	NCBI36
NG_016617.1:g.35891del , LRG_788:g.35891del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.961del MANE Select	ENSP00000251810.3:p.Thr321GlnfsTer?
ENST00000251810.7:c.961del	ENSP00000251810.3:p.Thr321GlnfsTer?
ENST00000395910.6:n.348del
ENST00000395912.6:c.805del	ENSP00000379248.2:p.Thr269GlnfsTer?
ENST00000519317.5:c.325del	ENSP00000430641.1:p.Thr109GlnfsTer?
ENST00000519962.5:c.106del	ENSP00000429140.1:p.Thr36GlnfsTer?
ENST00000522368.5:c.1130del
ENST00000522394.1:c.294del	ENSP00000429578.1:n.294del
ENST00000621845.1:c.799del	ENSP00000484318.1:p.Thr267GlnfsTer?
NM_001172477.1:c.1177del , LRG_788t1:c.1177del	NP_001165948.1:p.Thr393GlnfsTer?
NM_001172478.1:c.805del	NP_001165949.1:p.Thr269GlnfsTer?
NM_015713.4:c.961del , LRG_788t2:c.961del	NP_056528.2:p.Thr321GlnfsTer?
NM_001172478.2:c.805del	NP_001165949.1:p.Thr269GlnfsTer?
NM_015713.5:c.961del MANE Select	NP_056528.2:p.Thr321GlnfsTer?