Canonical Allele Identifier: CA413496503

Gene: IL2RG

Linked Data

• ClinVar Variation Id: 870713
• ClinVar RCV Id: RCV001090305
• dbSNP Id: rs111033621
• MyVariant Identifiers: chrX:g.70330142A>G (hg19) ; chrX:g.71110292A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110292A>G , CM000685.2:g.71110292A>G	GRCh38
NC_000023.10:g.70330142A>G , CM000685.1:g.70330142A>G	GRCh37
NC_000023.9:g.70246867A>G	NCBI36
NG_009088.1:g.6262T>C , LRG_150:g.6262T>C
NG_021141.1:g.1497T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000482750.6:c.458T>C	ENSP00000421262.2:p.Ile153Thr
ENST00000696903.1:n.509T>C
ENST00000374202.7:c.458T>C MANE Select	ENSP00000363318.3:p.Ile153Thr
ENST00000642473.1:n.822T>C
ENST00000644022.1:n.860+212T>C
ENST00000644708.1:n.864T>C
ENST00000644911.1:n.864T>C
ENST00000645266.1:c.458T>C	ENSP00000493734.1:p.Ile153Thr
ENST00000645518.1:c.458T>C	ENSP00000493986.1:p.Ile153Thr
ENST00000646106.1:c.458T>C	ENSP00000496437.1:p.Ile153Thr
ENST00000646505.1:c.458T>C	ENSP00000496673.1:p.Ile153Thr
ENST00000647492.1:c.458T>C	ENSP00000495340.1:p.Ile153Thr
ENST00000276110.6:n.1051T>C
ENST00000374188.7:c.-259T>C	ENSP00000363303.3:n.-259T>C
ENST00000374202.6:c.458T>C	ENSP00000363318.2:p.Ile153Thr
ENST00000456850.6:c.25-902T>C	ENSP00000388967.2:n.25-902T>C
ENST00000464642.5:c.326T>C	ENSP00000425233.1:p.Ile109Thr
ENST00000487883.1:c.422T>C	ENSP00000423966.1:p.Ile141Thr
ENST00000512747.3:n.521+212T>C
NM_000206.2:c.458T>C , LRG_150t1:c.458T>C	NP_000197.1:p.Ile153Thr
NM_000206.3:c.458T>C MANE Select	NP_000197.1:p.Ile153Thr