Canonical Allele Identifier: CA752898105

Gene: IL2RB

Linked Data

• dbSNP Id: rs769307076
• MyVariant Identifiers: chr22:g.37551678C>T (hg19) ; chr22:g.37155638C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37155638C>T , CM000684.2:g.37155638C>T	GRCh38
NC_000022.10:g.37551678C>T , CM000684.1:g.37551678C>T	GRCh37
NC_000022.9:g.35881624C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.-33-11433G>A	ENSP00000402685.2:n.-33-11433G>A
ENST00000445595.2:c.-34+6155G>A	ENSP00000401020.2:n.-34+6155G>A
ENST00000453962.6:c.-33-11433G>A	ENSP00000403731.2:n.-33-11433G>A
ENST00000698883.1:c.-34+637G>A	ENSP00000514005.1:n.-34+637G>A
ENST00000698892.1:c.-34+637G>A	ENSP00000514011.1:n.-34+637G>A
ENST00000698893.1:c.-34+637G>A	ENSP00000514012.1:n.-34+637G>A
ENST00000429622.5:c.-33-11433G>A	ENSP00000402685.1:n.-33-11433G>A
ENST00000445595.1:c.-34+6155G>A	ENSP00000401020.1:n.-34+6155G>A
ENST00000453962.5:c.-33-11433G>A	ENSP00000403731.1:n.-33-11433G>A
ENST00000461607.5:n.98-11433G>A
NM_001346222.1:c.-33-11433G>A	NP_001333151.1:n.-33-11433G>A
NM_001346223.1:c.-33-11433G>A	NP_001333152.1:n.-33-11433G>A
NM_001346223.2:c.-33-11433G>A	NP_001333152.1:n.-33-11433G>A