Canonical Allele Identifier: CA1025531409
Gene: IL2RB HGNC NCBI

Linked Data

dbSNP Id: rs1922647440

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37155474T>C , CM000684.2:g.37155474T>C GRCh38
NC_000022.10:g.37551514T>C , CM000684.1:g.37551514T>C GRCh37
NC_000022.9:g.35881460T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429622.6:c.-33-11269A>G ENSP00000402685.2:n.-33-11269A>G
ENST00000445595.2:c.-34+6319A>G ENSP00000401020.2:n.-34+6319A>G
ENST00000453962.6:c.-33-11269A>G ENSP00000403731.2:n.-33-11269A>G
ENST00000698883.1:c.-34+801A>G ENSP00000514005.1:n.-34+801A>G
ENST00000698892.1:c.-34+801A>G ENSP00000514011.1:n.-34+801A>G
ENST00000698893.1:c.-34+801A>G ENSP00000514012.1:n.-34+801A>G
ENST00000429622.5:c.-33-11269A>G ENSP00000402685.1:n.-33-11269A>G
ENST00000445595.1:c.-34+6319A>G ENSP00000401020.1:n.-34+6319A>G
ENST00000453962.5:c.-33-11269A>G ENSP00000403731.1:n.-33-11269A>G
ENST00000461607.5:n.98-11269A>G
NM_001346222.1:c.-33-11269A>G NP_001333151.1:n.-33-11269A>G
NM_001346223.1:c.-33-11269A>G NP_001333152.1:n.-33-11269A>G
NM_001346223.2:c.-33-11269A>G NP_001333152.1:n.-33-11269A>G