Canonical Allele Identifier: CA413497085

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330801C>T (hg19) ; chrX:g.71110951C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110951C>T , CM000685.2:g.71110951C>T	GRCh38
NC_000023.10:g.70330801C>T , CM000685.1:g.70330801C>T	GRCh37
NC_000023.9:g.70247526C>T	NCBI36
NG_009088.1:g.5603G>A , LRG_150:g.5603G>A
NG_021141.1:g.838G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.215G>A	ENSP00000421262.2:p.Cys72Tyr
ENST00000696903.1:n.266G>A
ENST00000374202.7:c.215G>A MANE Select	ENSP00000363318.3:p.Cys72Tyr
ENST00000642473.1:n.579G>A
ENST00000644022.1:n.621G>A
ENST00000644708.1:n.621G>A
ENST00000644911.1:n.621G>A
ENST00000645266.1:c.215G>A	ENSP00000493734.1:p.Cys72Tyr
ENST00000645518.1:c.215G>A	ENSP00000493986.1:p.Cys72Tyr
ENST00000646106.1:c.215G>A	ENSP00000496437.1:p.Cys72Tyr
ENST00000646505.1:c.215G>A	ENSP00000496673.1:p.Cys72Tyr
ENST00000647492.1:c.215G>A	ENSP00000495340.1:p.Cys72Tyr
ENST00000276110.6:n.600G>A
ENST00000374188.7:c.-502G>A	ENSP00000363303.3:n.-502G>A
ENST00000374202.6:c.215G>A	ENSP00000363318.2:p.Cys72Tyr
ENST00000456850.6:c.24+474G>A	ENSP00000388967.2:n.24+474G>A
ENST00000464642.5:c.83G>A	ENSP00000425233.1:p.Cys28Tyr
ENST00000473378.1:c.152G>A	ENSP00000423601.1:p.Cys51Tyr
ENST00000487883.1:c.179G>A	ENSP00000423966.1:p.Cys60Tyr
ENST00000512747.3:n.282G>A
NM_000206.2:c.215G>A , LRG_150t1:c.215G>A	NP_000197.1:p.Cys72Tyr
NM_000206.3:c.215G>A MANE Select	NP_000197.1:p.Cys72Tyr