Canonical Allele Identifier: CA411425101

Gene: IL2RB

Linked Data

• MyVariant Identifiers: chr22:g.37524623T>A (hg19) ; chr22:g.37128583T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37128583T>A , CM000684.2:g.37128583T>A	GRCh38
NC_000022.10:g.37524623T>A , CM000684.1:g.37524623T>A	GRCh37
NC_000022.9:g.35854569T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.1169A>T	ENSP00000402685.2:p.Glu390Val
ENST00000445595.2:c.1169A>T	ENSP00000401020.2:p.Glu390Val
ENST00000453962.6:c.1169A>T	ENSP00000403731.2:p.Glu390Val
ENST00000698883.1:c.1169A>T	ENSP00000514005.1:p.Glu390Val
ENST00000698890.1:c.1169A>T	ENSP00000514009.1:p.Glu390Val
ENST00000698891.1:c.*1161A>T	ENSP00000514010.1:n.*1161A>T
ENST00000698892.1:c.1169A>T	ENSP00000514011.1:p.Glu390Val
ENST00000698893.1:c.1169A>T	ENSP00000514012.1:p.Glu390Val
ENST00000698894.1:c.1187A>T	ENSP00000514013.1:p.Glu396Val
ENST00000698895.1:c.*969A>T	ENSP00000514014.1:n.*969A>T
ENST00000698896.1:c.*928A>T	ENSP00000514015.1:n.*928A>T
ENST00000698902.1:c.1166A>T	ENSP00000514017.1:p.Glu389Val
ENST00000698903.1:c.1166A>T	ENSP00000514018.1:p.Glu389Val
ENST00000698904.1:c.1142A>T	ENSP00000514019.1:p.Glu381Val
ENST00000698905.1:c.*343A>T	ENSP00000514020.1:n.*343A>T
ENST00000703410.1:c.903+3801A>T	ENSP00000516411.1:n.903+3801A>T
ENST00000216223.10:c.1169A>T MANE Select	ENSP00000216223.5:p.Glu390Val
ENST00000216223.9:c.1169A>T	ENSP00000216223.5:p.Glu390Val
ENST00000483573.1:n.647A>T
NM_000878.3:c.1169A>T	NP_000869.1:p.Glu390Val
NM_000878.4:c.1169A>T	NP_000869.1:p.Glu390Val
NM_001346222.1:c.1169A>T	NP_001333151.1:p.Glu390Val
NM_001346223.1:c.1169A>T	NP_001333152.1:p.Glu390Val
NM_000878.5:c.1169A>T MANE Select	NP_000869.1:p.Glu390Val
NM_001346223.2:c.1169A>T	NP_001333152.1:p.Glu390Val