Canonical Allele Identifier: CA413497110

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330810T>G (hg19) ; chrX:g.71110960T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110960T>G , CM000685.2:g.71110960T>G	GRCh38
NC_000023.10:g.70330810T>G , CM000685.1:g.70330810T>G	GRCh37
NC_000023.9:g.70247535T>G	NCBI36
NG_009088.1:g.5594A>C , LRG_150:g.5594A>C
NG_021141.1:g.829A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.206A>C	ENSP00000421262.2:p.Tyr69Ser
ENST00000696903.1:n.257A>C
ENST00000374202.7:c.206A>C MANE Select	ENSP00000363318.3:p.Tyr69Ser
ENST00000642473.1:n.570A>C
ENST00000644022.1:n.612A>C
ENST00000644708.1:n.612A>C
ENST00000644911.1:n.612A>C
ENST00000645266.1:c.206A>C	ENSP00000493734.1:p.Tyr69Ser
ENST00000645518.1:c.206A>C	ENSP00000493986.1:p.Tyr69Ser
ENST00000646106.1:c.206A>C	ENSP00000496437.1:p.Tyr69Ser
ENST00000646505.1:c.206A>C	ENSP00000496673.1:p.Tyr69Ser
ENST00000647492.1:c.206A>C	ENSP00000495340.1:p.Tyr69Ser
ENST00000276110.6:n.591A>C
ENST00000374188.7:c.-511A>C	ENSP00000363303.3:n.-511A>C
ENST00000374202.6:c.206A>C	ENSP00000363318.2:p.Tyr69Ser
ENST00000456850.6:c.24+465A>C	ENSP00000388967.2:n.24+465A>C
ENST00000464642.5:c.74A>C	ENSP00000425233.1:p.Tyr25Ser
ENST00000473378.1:c.143A>C	ENSP00000423601.1:p.Tyr48Ser
ENST00000487883.1:c.170A>C	ENSP00000423966.1:p.Tyr57Ser
ENST00000512747.3:n.273A>C
NM_000206.2:c.206A>C , LRG_150t1:c.206A>C	NP_000197.1:p.Tyr69Ser
NM_000206.3:c.206A>C MANE Select	NP_000197.1:p.Tyr69Ser