Canonical Allele Identifier: CA2404206801

Gene: IL2RB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37148476T= , CM000684.2:g.37148476T=	GRCh38
NC_000022.10:g.37544516T= , CM000684.1:g.37544516T=	GRCh37
NC_000022.9:g.35874462T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.-33-4271A=	ENSP00000402685.2:n.-33-4271A=
ENST00000445595.2:c.-33-4271A=	ENSP00000401020.2:n.-33-4271A=
ENST00000453962.6:c.-33-4271A=	ENSP00000403731.2:n.-33-4271A=
ENST00000698883.1:c.-33-4271A=	ENSP00000514005.1:n.-33-4271A=
ENST00000698891.1:c.-34+1349A=	ENSP00000514010.1:n.-34+1349A=
ENST00000698892.1:c.-33-4271A=	ENSP00000514011.1:n.-33-4271A=
ENST00000698893.1:c.-33-4271A=	ENSP00000514012.1:n.-33-4271A=
ENST00000698894.1:c.-34+1349A=	ENSP00000514013.1:n.-34+1349A=
ENST00000698895.1:c.-34+1349A=	ENSP00000514014.1:n.-34+1349A=
ENST00000698898.1:n.73+1349A=
ENST00000698902.1:c.-34+1349A=	ENSP00000514017.1:n.-34+1349A=
ENST00000698903.1:c.-34+1349A=	ENSP00000514018.1:n.-34+1349A=
ENST00000698904.1:c.-34+1349A=	ENSP00000514019.1:n.-34+1349A=
ENST00000698905.1:c.-34+1349A=	ENSP00000514020.1:n.-34+1349A=
ENST00000703410.1:c.-34+1349A=	ENSP00000516411.1:n.-34+1349A=
ENST00000216223.10:c.-34+1349A= MANE Select	ENSP00000216223.5:n.-34+1349A=
ENST00000216223.9:c.-34+1349A=	ENSP00000216223.5:n.-34+1349A=
ENST00000429622.5:c.-33-4271A=	ENSP00000402685.1:n.-33-4271A=
ENST00000445595.1:c.-33-4271A=	ENSP00000401020.1:n.-33-4271A=
ENST00000453962.5:c.-33-4271A=	ENSP00000403731.1:n.-33-4271A=
ENST00000461607.5:n.98-4271A=
NM_000878.3:c.-34+1349A=	NP_000869.1:n.-34+1349A=
NM_000878.4:c.-34+1349A=	NP_000869.1:n.-34+1349A=
NM_001346222.1:c.-33-4271A=	NP_001333151.1:n.-33-4271A=
NM_001346223.1:c.-33-4271A=	NP_001333152.1:n.-33-4271A=
NM_000878.5:c.-34+1349A= MANE Select	NP_000869.1:n.-34+1349A=
NM_001346223.2:c.-33-4271A=	NP_001333152.1:n.-33-4271A=