Canonical Allele Identifier: CA1806686069

Gene: RRM2B

Linked Data

• dbSNP Id: rs1441587875

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231898_102231901del , CM000670.2:g.102231898_102231901del	GRCh38
NC_000008.10:g.103244126_103244129del , CM000670.1:g.103244126_103244129del	GRCh37
NC_000008.9:g.103313302_103313305del	NCBI36
NG_016617.1:g.12222_12225del , LRG_788:g.12222_12225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+252_204+255del MANE Select	ENSP00000251810.3:n.204+252_204+255del
ENST00000251810.7:c.204+252_204+255del	ENSP00000251810.3:n.204+252_204+255del
ENST00000395912.6:c.49-5863_49-5860del	ENSP00000379248.2:n.49-5863_49-5860del
ENST00000517517.1:n.513+252_513+255del
ENST00000519317.5:c.48+6930_48+6933del	ENSP00000430641.1:n.48+6930_48+6933del
ENST00000519962.5:c.48+6930_48+6933del	ENSP00000429140.1:n.48+6930_48+6933del
ENST00000522368.5:c.373+252_373+255del
ENST00000522394.1:c.122+334_122+337del	ENSP00000429578.1:n.122+334_122+337del
ENST00000523957.1:c.*127+252_*127+255del	ENSP00000427830.1:n.*127+252_*127+255del
ENST00000621845.1:c.42+252_42+255del	ENSP00000484318.1:n.42+252_42+255del
NM_001172477.1:c.420+252_420+255del , LRG_788t1:c.420+252_420+255del	NP_001165948.1:n.420+252_420+255del
NM_001172478.1:c.49-5863_49-5860del	NP_001165949.1:n.49-5863_49-5860del
NM_015713.4:c.204+252_204+255del , LRG_788t2:c.204+252_204+255del	NP_056528.2:n.204+252_204+255del
NM_001172478.2:c.49-5863_49-5860del	NP_001165949.1:n.49-5863_49-5860del
NM_015713.5:c.204+252_204+255del MANE Select	NP_056528.2:n.204+252_204+255del