Canonical Allele Identifier: CA2404197585

Gene: IL2RB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37128589G= , CM000684.2:g.37128589G=	GRCh38
NC_000022.10:g.37524629G= , CM000684.1:g.37524629G=	GRCh37
NC_000022.9:g.35854575G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.1163C=	ENSP00000402685.2:p.Ser388=
ENST00000445595.2:c.1163C=	ENSP00000401020.2:p.Ser388=
ENST00000453962.6:c.1163C=	ENSP00000403731.2:p.Ser388=
ENST00000698883.1:c.1163C=	ENSP00000514005.1:p.Ser388=
ENST00000698890.1:c.1163C=	ENSP00000514009.1:p.Ser388=
ENST00000698891.1:c.*1155C=	ENSP00000514010.1:n.*1155C=
ENST00000698892.1:c.1163C=	ENSP00000514011.1:p.Ser388=
ENST00000698893.1:c.1163C=	ENSP00000514012.1:p.Ser388=
ENST00000698894.1:c.1181C=	ENSP00000514013.1:p.Ser394=
ENST00000698895.1:c.*963C=	ENSP00000514014.1:n.*963C=
ENST00000698896.1:c.*922C=	ENSP00000514015.1:n.*922C=
ENST00000698902.1:c.1160C=	ENSP00000514017.1:p.Ser387=
ENST00000698903.1:c.1160C=	ENSP00000514018.1:p.Ser387=
ENST00000698904.1:c.1136C=	ENSP00000514019.1:p.Ser379=
ENST00000698905.1:c.*337C=	ENSP00000514020.1:n.*337C=
ENST00000703410.1:c.903+3795C=	ENSP00000516411.1:n.903+3795C=
ENST00000216223.10:c.1163C= MANE Select	ENSP00000216223.5:p.Ser388=
ENST00000216223.9:c.1163C=	ENSP00000216223.5:p.Ser388=
ENST00000483573.1:n.641C=
NM_000878.3:c.1163C=	NP_000869.1:p.Ser388=
NM_000878.4:c.1163C=	NP_000869.1:p.Ser388=
NM_001346222.1:c.1163C=	NP_001333151.1:p.Ser388=
NM_001346223.1:c.1163C=	NP_001333152.1:p.Ser388=
NM_000878.5:c.1163C= MANE Select	NP_000869.1:p.Ser388=
NM_001346223.2:c.1163C=	NP_001333152.1:p.Ser388=