Canonical Allele Identifier: CA1806686135

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811039258

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102232036_102232037del , CM000670.2:g.102232036_102232037del	GRCh38
NC_000008.10:g.103244264_103244265del , CM000670.1:g.103244264_103244265del	GRCh37
NC_000008.9:g.103313440_103313441del	NCBI36
NG_016617.1:g.12083_12084del , LRG_788:g.12083_12084del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+113_204+114del MANE Select	ENSP00000251810.3:n.204+113_204+114del
ENST00000251810.7:c.204+113_204+114del	ENSP00000251810.3:n.204+113_204+114del
ENST00000395912.6:c.49-6002_49-6001del	ENSP00000379248.2:n.49-6002_49-6001del
ENST00000517517.1:n.513+113_513+114del
ENST00000519317.5:c.48+6791_48+6792del	ENSP00000430641.1:n.48+6791_48+6792del
ENST00000519962.5:c.48+6791_48+6792del	ENSP00000429140.1:n.48+6791_48+6792del
ENST00000522368.5:c.373+113_373+114del
ENST00000522394.1:c.122+195_122+196del	ENSP00000429578.1:n.122+195_122+196del
ENST00000523957.1:c.*127+113_*127+114del	ENSP00000427830.1:n.*127+113_*127+114del
ENST00000621845.1:c.42+113_42+114del	ENSP00000484318.1:n.42+113_42+114del
NM_001172477.1:c.420+113_420+114del , LRG_788t1:c.420+113_420+114del	NP_001165948.1:n.420+113_420+114del
NM_001172478.1:c.49-6002_49-6001del	NP_001165949.1:n.49-6002_49-6001del
NM_015713.4:c.204+113_204+114del , LRG_788t2:c.204+113_204+114del	NP_056528.2:n.204+113_204+114del
NM_001172478.2:c.49-6002_49-6001del	NP_001165949.1:n.49-6002_49-6001del
NM_015713.5:c.204+113_204+114del MANE Select	NP_056528.2:n.204+113_204+114del