Canonical Allele Identifier: CA1025522711

Gene: IL2RB

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37137994G>C , CM000684.2:g.37137994G>C	GRCh38
NC_000022.10:g.37534034G>C , CM000684.1:g.37534034G>C	GRCh37
NC_000022.9:g.35863980G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429622.6:c.389-259C>G	ENSP00000402685.2:n.389-259C>G
ENST00000445595.2:c.389-259C>G	ENSP00000401020.2:n.389-259C>G
ENST00000453962.6:c.389-259C>G	ENSP00000403731.2:n.389-259C>G
ENST00000698883.1:c.389-259C>G	ENSP00000514005.1:n.389-259C>G
ENST00000698890.1:c.389-259C>G	ENSP00000514009.1:n.389-259C>G
ENST00000698891.1:c.*381-259C>G	ENSP00000514010.1:n.*381-259C>G
ENST00000698892.1:c.389-259C>G	ENSP00000514011.1:n.389-259C>G
ENST00000698893.1:c.389-259C>G	ENSP00000514012.1:n.389-259C>G
ENST00000698894.1:c.407-259C>G	ENSP00000514013.1:n.407-259C>G
ENST00000698895.1:c.*189-259C>G	ENSP00000514014.1:n.*189-259C>G
ENST00000698896.1:c.*151-259C>G	ENSP00000514015.1:n.*151-259C>G
ENST00000698897.1:n.315-259C>G
ENST00000698898.1:n.1518C>G
ENST00000698902.1:c.389-259C>G	ENSP00000514017.1:n.389-259C>G
ENST00000698903.1:c.389-259C>G	ENSP00000514018.1:n.389-259C>G
ENST00000698904.1:c.389-259C>G	ENSP00000514019.1:n.389-259C>G
ENST00000698905.1:c.389-259C>G	ENSP00000514020.1:n.389-259C>G
ENST00000703410.1:c.389-259C>G	ENSP00000516411.1:n.389-259C>G
ENST00000216223.10:c.389-259C>G MANE Select	ENSP00000216223.5:n.389-259C>G
ENST00000216223.9:c.389-259C>G	ENSP00000216223.5:n.389-259C>G
ENST00000429622.5:c.389-259C>G	ENSP00000402685.1:n.389-259C>G
ENST00000453962.5:c.389-259C>G	ENSP00000403731.1:n.389-259C>G
NM_000878.3:c.389-259C>G	NP_000869.1:n.389-259C>G
NM_000878.4:c.389-259C>G	NP_000869.1:n.389-259C>G
NM_001346222.1:c.389-259C>G	NP_001333151.1:n.389-259C>G
NM_001346223.1:c.389-259C>G	NP_001333152.1:n.389-259C>G
NM_000878.5:c.389-259C>G MANE Select	NP_000869.1:n.389-259C>G
NM_001346223.2:c.389-259C>G	NP_001333152.1:n.389-259C>G