Canonical Allele Identifier: CA1025524758

Gene: IL2RB

Linked Data

• dbSNP Id: rs1922042535
• gnomAD v3: 22-37142998-G-A
• gnomAD v4: 22-37142998-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37142998G>A , CM000684.2:g.37142998G>A	GRCh38
NC_000022.10:g.37539038G>A , CM000684.1:g.37539038G>A	GRCh37
NC_000022.9:g.35868984G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.204-486C>T	ENSP00000402685.2:n.204-486C>T
ENST00000440958.2:c.204-247C>T	ENSP00000400416.2:n.204-247C>T
ENST00000445595.2:c.204-486C>T	ENSP00000401020.2:n.204-486C>T
ENST00000453962.6:c.204-486C>T	ENSP00000403731.2:n.204-486C>T
ENST00000698883.1:c.204-486C>T	ENSP00000514005.1:n.204-486C>T
ENST00000698890.1:c.204-486C>T	ENSP00000514009.1:n.204-486C>T
ENST00000698891.1:c.*196-486C>T	ENSP00000514010.1:n.*196-486C>T
ENST00000698892.1:c.204-486C>T	ENSP00000514011.1:n.204-486C>T
ENST00000698893.1:c.204-486C>T	ENSP00000514012.1:n.204-486C>T
ENST00000698894.1:c.204-468C>T	ENSP00000514013.1:n.204-468C>T
ENST00000698895.1:c.204-437C>T	ENSP00000514014.1:n.204-437C>T
ENST00000698896.1:c.204-466C>T	ENSP00000514015.1:n.204-466C>T
ENST00000698897.1:n.130-486C>T
ENST00000698898.1:n.310-486C>T
ENST00000698902.1:c.204-486C>T	ENSP00000514017.1:n.204-486C>T
ENST00000698903.1:c.204-486C>T	ENSP00000514018.1:n.204-486C>T
ENST00000698904.1:c.204-486C>T	ENSP00000514019.1:n.204-486C>T
ENST00000698905.1:c.204-486C>T	ENSP00000514020.1:n.204-486C>T
ENST00000703410.1:c.204-486C>T	ENSP00000516411.1:n.204-486C>T
ENST00000216223.10:c.204-486C>T MANE Select	ENSP00000216223.5:n.204-486C>T
ENST00000216223.9:c.204-486C>T	ENSP00000216223.5:n.204-486C>T
ENST00000429622.5:c.204-486C>T	ENSP00000402685.1:n.204-486C>T
ENST00000440958.1:c.102-247C>T	ENSP00000400416.1:n.102-247C>T
ENST00000445595.1:c.204-486C>T	ENSP00000401020.1:n.204-486C>T
ENST00000453962.5:c.204-486C>T	ENSP00000403731.1:n.204-486C>T
ENST00000461607.5:n.334-486C>T
NM_000878.3:c.204-486C>T	NP_000869.1:n.204-486C>T
NM_000878.4:c.204-486C>T	NP_000869.1:n.204-486C>T
NM_001346222.1:c.204-486C>T	NP_001333151.1:n.204-486C>T
NM_001346223.1:c.204-486C>T	NP_001333152.1:n.204-486C>T
NM_000878.5:c.204-486C>T MANE Select	NP_000869.1:n.204-486C>T
NM_001346223.2:c.204-486C>T	NP_001333152.1:n.204-486C>T