Canonical Allele Identifier: CA411425121

Gene: IL2RB

Linked Data

• MyVariant Identifiers: chr22:g.37524631G>C (hg19) ; chr22:g.37128591G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37128591G>C , CM000684.2:g.37128591G>C	GRCh38
NC_000022.10:g.37524631G>C , CM000684.1:g.37524631G>C	GRCh37
NC_000022.9:g.35854577G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429622.6:c.1161C>G	ENSP00000402685.2:p.Tyr387Ter
ENST00000445595.2:c.1161C>G	ENSP00000401020.2:p.Tyr387Ter
ENST00000453962.6:c.1161C>G	ENSP00000403731.2:p.Tyr387Ter
ENST00000698883.1:c.1161C>G	ENSP00000514005.1:p.Tyr387Ter
ENST00000698890.1:c.1161C>G	ENSP00000514009.1:p.Tyr387Ter
ENST00000698891.1:c.*1153C>G	ENSP00000514010.1:n.*1153C>G
ENST00000698892.1:c.1161C>G	ENSP00000514011.1:p.Tyr387Ter
ENST00000698893.1:c.1161C>G	ENSP00000514012.1:p.Tyr387Ter
ENST00000698894.1:c.1179C>G	ENSP00000514013.1:p.Tyr393Ter
ENST00000698895.1:c.*961C>G	ENSP00000514014.1:n.*961C>G
ENST00000698896.1:c.*920C>G	ENSP00000514015.1:n.*920C>G
ENST00000698902.1:c.1158C>G	ENSP00000514017.1:p.Tyr386Ter
ENST00000698903.1:c.1158C>G	ENSP00000514018.1:p.Tyr386Ter
ENST00000698904.1:c.1134C>G	ENSP00000514019.1:p.Tyr378Ter
ENST00000698905.1:c.*335C>G	ENSP00000514020.1:n.*335C>G
ENST00000703410.1:c.903+3793C>G	ENSP00000516411.1:n.903+3793C>G
ENST00000216223.10:c.1161C>G MANE Select	ENSP00000216223.5:p.Tyr387Ter
ENST00000216223.9:c.1161C>G	ENSP00000216223.5:p.Tyr387Ter
ENST00000483573.1:n.639C>G
NM_000878.3:c.1161C>G	NP_000869.1:p.Tyr387Ter
NM_000878.4:c.1161C>G	NP_000869.1:p.Tyr387Ter
NM_001346222.1:c.1161C>G	NP_001333151.1:p.Tyr387Ter
NM_001346223.1:c.1161C>G	NP_001333152.1:p.Tyr387Ter
NM_000878.5:c.1161C>G MANE Select	NP_000869.1:p.Tyr387Ter
NM_001346223.2:c.1161C>G	NP_001333152.1:p.Tyr387Ter