Canonical Allele Identifier: CA2404210021
Gene: IL2RB HGNC NCBI

Linked Data

dbSNP Id: rs1922649199

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37155511G>A , CM000684.2:g.37155511G>A GRCh38
NC_000022.10:g.37551551G>A , CM000684.1:g.37551551G>A GRCh37
NC_000022.9:g.35881497G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429622.6:c.-33-11306C>T ENSP00000402685.2:n.-33-11306C>T
ENST00000445595.2:c.-34+6282C>T ENSP00000401020.2:n.-34+6282C>T
ENST00000453962.6:c.-33-11306C>T ENSP00000403731.2:n.-33-11306C>T
ENST00000698883.1:c.-34+764C>T ENSP00000514005.1:n.-34+764C>T
ENST00000698892.1:c.-34+764C>T ENSP00000514011.1:n.-34+764C>T
ENST00000698893.1:c.-34+764C>T ENSP00000514012.1:n.-34+764C>T
ENST00000429622.5:c.-33-11306C>T ENSP00000402685.1:n.-33-11306C>T
ENST00000445595.1:c.-34+6282C>T ENSP00000401020.1:n.-34+6282C>T
ENST00000453962.5:c.-33-11306C>T ENSP00000403731.1:n.-33-11306C>T
ENST00000461607.5:n.98-11306C>T
NM_001346222.1:c.-33-11306C>T NP_001333151.1:n.-33-11306C>T
NM_001346223.1:c.-33-11306C>T NP_001333152.1:n.-33-11306C>T
NM_001346223.2:c.-33-11306C>T NP_001333152.1:n.-33-11306C>T