Canonical Allele Identifier: CA1025531486

Gene: IL2RB

Linked Data

• gnomAD v3: 22-37155644-C-T
• gnomAD v4: 22-37155644-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37155644C>T , CM000684.2:g.37155644C>T	GRCh38
NC_000022.10:g.37551684C>T , CM000684.1:g.37551684C>T	GRCh37
NC_000022.9:g.35881630C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429622.6:c.-33-11439G>A	ENSP00000402685.2:n.-33-11439G>A
ENST00000445595.2:c.-34+6149G>A	ENSP00000401020.2:n.-34+6149G>A
ENST00000453962.6:c.-33-11439G>A	ENSP00000403731.2:n.-33-11439G>A
ENST00000698883.1:c.-34+631G>A	ENSP00000514005.1:n.-34+631G>A
ENST00000698892.1:c.-34+631G>A	ENSP00000514011.1:n.-34+631G>A
ENST00000698893.1:c.-34+631G>A	ENSP00000514012.1:n.-34+631G>A
ENST00000429622.5:c.-33-11439G>A	ENSP00000402685.1:n.-33-11439G>A
ENST00000445595.1:c.-34+6149G>A	ENSP00000401020.1:n.-34+6149G>A
ENST00000453962.5:c.-33-11439G>A	ENSP00000403731.1:n.-33-11439G>A
ENST00000461607.5:n.98-11439G>A
NM_001346222.1:c.-33-11439G>A	NP_001333151.1:n.-33-11439G>A
NM_001346223.1:c.-33-11439G>A	NP_001333152.1:n.-33-11439G>A
NM_001346223.2:c.-33-11439G>A	NP_001333152.1:n.-33-11439G>A