Canonical Allele Identifier: CA2499226826

Gene: IL2RG

Linked Data

• ClinVar Variation Id: 1133674
• ClinVar RCV Id: RCV001468309
• dbSNP Id: rs886039387

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110703T>A , CM000685.2:g.71110703T>A	GRCh38
NC_000023.10:g.70330553T>A , CM000685.1:g.70330553T>A	GRCh37
NC_000023.9:g.70247278T>A	NCBI36
NG_009088.1:g.5851A>T , LRG_150:g.5851A>T
NG_021141.1:g.1086A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.270-15A>T	ENSP00000421262.2:n.270-15A>T
ENST00000696903.1:n.321-15A>T
ENST00000374202.7:c.270-15A>T MANE Select	ENSP00000363318.3:n.270-15A>T
ENST00000642473.1:n.634-15A>T
ENST00000644022.1:n.676-15A>T
ENST00000644708.1:n.676-15A>T
ENST00000644911.1:n.676-15A>T
ENST00000645266.1:c.270-15A>T	ENSP00000493734.1:n.270-15A>T
ENST00000645518.1:c.270-15A>T	ENSP00000493986.1:n.270-15A>T
ENST00000646106.1:c.270-15A>T	ENSP00000496437.1:n.270-15A>T
ENST00000646505.1:c.270-15A>T	ENSP00000496673.1:n.270-15A>T
ENST00000647492.1:c.270-15A>T	ENSP00000495340.1:n.270-15A>T
ENST00000276110.6:n.655-15A>T
ENST00000374188.7:c.-447-15A>T	ENSP00000363303.3:n.-447-15A>T
ENST00000374202.6:c.270-15A>T	ENSP00000363318.2:n.270-15A>T
ENST00000456850.6:c.24+722A>T	ENSP00000388967.2:n.24+722A>T
ENST00000464642.5:c.138-15A>T	ENSP00000425233.1:n.138-15A>T
ENST00000473378.1:c.207-15A>T	ENSP00000423601.1:n.207-15A>T
ENST00000487883.1:c.234-15A>T	ENSP00000423966.1:n.234-15A>T
ENST00000512747.3:n.337-15A>T
NM_000206.2:c.270-15A>T , LRG_150t1:c.270-15A>T	NP_000197.1:n.270-15A>T
NM_000206.3:c.270-15A>T MANE Select	NP_000197.1:n.270-15A>T