Canonical Allele Identifier: CA2656494484
Gene: IL2RB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37142894G>T , CM000684.2:g.37142894G>T GRCh38
NC_000022.10:g.37538934G>T , CM000684.1:g.37538934G>T GRCh37
NC_000022.9:g.35868880G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429622.6:c.204-382C>A ENSP00000402685.2:n.204-382C>A
ENST00000440958.2:c.204-143C>A ENSP00000400416.2:n.204-143C>A
ENST00000445595.2:c.204-382C>A ENSP00000401020.2:n.204-382C>A
ENST00000453962.6:c.204-382C>A ENSP00000403731.2:n.204-382C>A
ENST00000698883.1:c.204-382C>A ENSP00000514005.1:n.204-382C>A
ENST00000698890.1:c.204-382C>A ENSP00000514009.1:n.204-382C>A
ENST00000698891.1:c.*196-382C>A ENSP00000514010.1:n.*196-382C>A
ENST00000698892.1:c.204-382C>A ENSP00000514011.1:n.204-382C>A
ENST00000698893.1:c.204-382C>A ENSP00000514012.1:n.204-382C>A
ENST00000698894.1:c.204-364C>A ENSP00000514013.1:n.204-364C>A
ENST00000698895.1:c.204-333C>A ENSP00000514014.1:n.204-333C>A
ENST00000698896.1:c.204-362C>A ENSP00000514015.1:n.204-362C>A
ENST00000698897.1:n.130-382C>A
ENST00000698898.1:n.310-382C>A
ENST00000698902.1:c.204-382C>A ENSP00000514017.1:n.204-382C>A
ENST00000698903.1:c.204-382C>A ENSP00000514018.1:n.204-382C>A
ENST00000698904.1:c.204-382C>A ENSP00000514019.1:n.204-382C>A
ENST00000698905.1:c.204-382C>A ENSP00000514020.1:n.204-382C>A
ENST00000703410.1:c.204-382C>A ENSP00000516411.1:n.204-382C>A
ENST00000216223.10:c.204-382C>A MANE Select ENSP00000216223.5:n.204-382C>A
ENST00000216223.9:c.204-382C>A ENSP00000216223.5:n.204-382C>A
ENST00000429622.5:c.204-382C>A ENSP00000402685.1:n.204-382C>A
ENST00000440958.1:c.102-143C>A ENSP00000400416.1:n.102-143C>A
ENST00000445595.1:c.204-382C>A ENSP00000401020.1:n.204-382C>A
ENST00000453962.5:c.204-382C>A ENSP00000403731.1:n.204-382C>A
ENST00000461607.5:n.334-382C>A
NM_000878.3:c.204-382C>A NP_000869.1:n.204-382C>A
NM_000878.4:c.204-382C>A NP_000869.1:n.204-382C>A
NM_001346222.1:c.204-382C>A NP_001333151.1:n.204-382C>A
NM_001346223.1:c.204-382C>A NP_001333152.1:n.204-382C>A
NM_000878.5:c.204-382C>A MANE Select NP_000869.1:n.204-382C>A
NM_001346223.2:c.204-382C>A NP_001333152.1:n.204-382C>A