Canonical Allele Identifier: CA1806686110

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811038145

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231987_102231991del , CM000670.2:g.102231987_102231991del	GRCh38
NC_000008.10:g.103244215_103244219del , CM000670.1:g.103244215_103244219del	GRCh37
NC_000008.9:g.103313391_103313395del	NCBI36
NG_016617.1:g.12133_12137del , LRG_788:g.12133_12137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+163_204+167del MANE Select	ENSP00000251810.3:n.204+163_204+167del
ENST00000251810.7:c.204+163_204+167del	ENSP00000251810.3:n.204+163_204+167del
ENST00000395912.6:c.49-5952_49-5948del	ENSP00000379248.2:n.49-5952_49-5948del
ENST00000517517.1:n.513+163_513+167del
ENST00000519317.5:c.48+6841_48+6845del	ENSP00000430641.1:n.48+6841_48+6845del
ENST00000519962.5:c.48+6841_48+6845del	ENSP00000429140.1:n.48+6841_48+6845del
ENST00000522368.5:c.373+163_373+167del
ENST00000522394.1:c.122+245_122+249del	ENSP00000429578.1:n.122+245_122+249del
ENST00000523957.1:c.*127+163_*127+167del	ENSP00000427830.1:n.*127+163_*127+167del
ENST00000621845.1:c.42+163_42+167del	ENSP00000484318.1:n.42+163_42+167del
NM_001172477.1:c.420+163_420+167del , LRG_788t1:c.420+163_420+167del	NP_001165948.1:n.420+163_420+167del
NM_001172478.1:c.49-5952_49-5948del	NP_001165949.1:n.49-5952_49-5948del
NM_015713.4:c.204+163_204+167del , LRG_788t2:c.204+163_204+167del	NP_056528.2:n.204+163_204+167del
NM_001172478.2:c.49-5952_49-5948del	NP_001165949.1:n.49-5952_49-5948del
NM_015713.5:c.204+163_204+167del MANE Select	NP_056528.2:n.204+163_204+167del