Canonical Allele Identifier: CA1025531585

Gene: IL2RB

Linked Data

• dbSNP Id: rs1922667710
• gnomAD v3: 22-37155993-GCTGT-G
• gnomAD v4: 22-37155993-GCTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37155996_37155999del , CM000684.2:g.37155996_37155999del	GRCh38
NC_000022.10:g.37552036_37552039del , CM000684.1:g.37552036_37552039del	GRCh37
NC_000022.9:g.35881982_35881985del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429622.6:c.-33-11792_-33-11789del	ENSP00000402685.2:n.-33-11792_-33-11789del
ENST00000445595.2:c.-34+5796_-34+5799del	ENSP00000401020.2:n.-34+5796_-34+5799del
ENST00000453962.6:c.-33-11792_-33-11789del	ENSP00000403731.2:n.-33-11792_-33-11789del
ENST00000698883.1:c.-34+278_-34+281del	ENSP00000514005.1:n.-34+278_-34+281del
ENST00000698892.1:c.-34+278_-34+281del	ENSP00000514011.1:n.-34+278_-34+281del
ENST00000698893.1:c.-34+278_-34+281del	ENSP00000514012.1:n.-34+278_-34+281del
ENST00000429622.5:c.-33-11792_-33-11789del	ENSP00000402685.1:n.-33-11792_-33-11789del
ENST00000445595.1:c.-34+5796_-34+5799del	ENSP00000401020.1:n.-34+5796_-34+5799del
ENST00000453962.5:c.-33-11792_-33-11789del	ENSP00000403731.1:n.-33-11792_-33-11789del
ENST00000461607.5:n.98-11792_98-11789del
NM_001346222.1:c.-33-11792_-33-11789del	NP_001333151.1:n.-33-11792_-33-11789del
NM_001346223.1:c.-33-11792_-33-11789del	NP_001333152.1:n.-33-11792_-33-11789del
NM_001346223.2:c.-33-11792_-33-11789del	NP_001333152.1:n.-33-11792_-33-11789del