Canonical Allele Identifier: CA1025531523

Gene: IL2RB

Linked Data

• dbSNP Id: rs1922659124
• gnomAD v3: 22-37155771-GCTC-G
• gnomAD v4: 22-37155771-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37155773_37155775del , CM000684.2:g.37155773_37155775del	GRCh38
NC_000022.10:g.37551813_37551815del , CM000684.1:g.37551813_37551815del	GRCh37
NC_000022.9:g.35881759_35881761del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429622.6:c.-33-11569_-33-11567del	ENSP00000402685.2:n.-33-11569_-33-11567del
ENST00000445595.2:c.-34+6019_-34+6021del	ENSP00000401020.2:n.-34+6019_-34+6021del
ENST00000453962.6:c.-33-11569_-33-11567del	ENSP00000403731.2:n.-33-11569_-33-11567del
ENST00000698883.1:c.-34+501_-34+503del	ENSP00000514005.1:n.-34+501_-34+503del
ENST00000698892.1:c.-34+501_-34+503del	ENSP00000514011.1:n.-34+501_-34+503del
ENST00000698893.1:c.-34+501_-34+503del	ENSP00000514012.1:n.-34+501_-34+503del
ENST00000429622.5:c.-33-11569_-33-11567del	ENSP00000402685.1:n.-33-11569_-33-11567del
ENST00000445595.1:c.-34+6019_-34+6021del	ENSP00000401020.1:n.-34+6019_-34+6021del
ENST00000453962.5:c.-33-11569_-33-11567del	ENSP00000403731.1:n.-33-11569_-33-11567del
ENST00000461607.5:n.98-11569_98-11567del
NM_001346222.1:c.-33-11569_-33-11567del	NP_001333151.1:n.-33-11569_-33-11567del
NM_001346223.1:c.-33-11569_-33-11567del	NP_001333152.1:n.-33-11569_-33-11567del
NM_001346223.2:c.-33-11569_-33-11567del	NP_001333152.1:n.-33-11569_-33-11567del