Canonical Allele Identifier: CA1117286876

Gene: RRM2B

Linked Data

• dbSNP Id: rs1811038247
• gnomAD v3: 8-102231983-TAAACTA-T
• gnomAD v4: 8-102231983-TAAACTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.102231988_102231993del , CM000670.2:g.102231988_102231993del	GRCh38
NC_000008.10:g.103244216_103244221del , CM000670.1:g.103244216_103244221del	GRCh37
NC_000008.9:g.103313392_103313397del	NCBI36
NG_016617.1:g.12130_12135del , LRG_788:g.12130_12135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251810.8:c.204+160_204+165del MANE Select	ENSP00000251810.3:n.204+160_204+165del
ENST00000251810.7:c.204+160_204+165del	ENSP00000251810.3:n.204+160_204+165del
ENST00000395912.6:c.49-5955_49-5950del	ENSP00000379248.2:n.49-5955_49-5950del
ENST00000517517.1:n.513+160_513+165del
ENST00000519317.5:c.48+6838_48+6843del	ENSP00000430641.1:n.48+6838_48+6843del
ENST00000519962.5:c.48+6838_48+6843del	ENSP00000429140.1:n.48+6838_48+6843del
ENST00000522368.5:c.373+160_373+165del
ENST00000522394.1:c.122+242_122+247del	ENSP00000429578.1:n.122+242_122+247del
ENST00000523957.1:c.*127+160_*127+165del	ENSP00000427830.1:n.*127+160_*127+165del
ENST00000621845.1:c.42+160_42+165del	ENSP00000484318.1:n.42+160_42+165del
NM_001172477.1:c.420+160_420+165del , LRG_788t1:c.420+160_420+165del	NP_001165948.1:n.420+160_420+165del
NM_001172478.1:c.49-5955_49-5950del	NP_001165949.1:n.49-5955_49-5950del
NM_015713.4:c.204+160_204+165del , LRG_788t2:c.204+160_204+165del	NP_056528.2:n.204+160_204+165del
NM_001172478.2:c.49-5955_49-5950del	NP_001165949.1:n.49-5955_49-5950del
NM_015713.5:c.204+160_204+165del MANE Select	NP_056528.2:n.204+160_204+165del