Canonical Allele Identifier: CA413497154

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330829A>C (hg19) ; chrX:g.71110979A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110979A>C , CM000685.2:g.71110979A>C	GRCh38
NC_000023.10:g.70330829A>C , CM000685.1:g.70330829A>C	GRCh37
NC_000023.9:g.70247554A>C	NCBI36
NG_009088.1:g.5575T>G , LRG_150:g.5575T>G
NG_021141.1:g.810T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.187T>G	ENSP00000421262.2:p.Phe63Val
ENST00000696903.1:n.238T>G
ENST00000374202.7:c.187T>G MANE Select	ENSP00000363318.3:p.Phe63Val
ENST00000642473.1:n.551T>G
ENST00000644022.1:n.593T>G
ENST00000644708.1:n.593T>G
ENST00000644911.1:n.593T>G
ENST00000645266.1:c.187T>G	ENSP00000493734.1:p.Phe63Val
ENST00000645518.1:c.187T>G	ENSP00000493986.1:p.Phe63Val
ENST00000646106.1:c.187T>G	ENSP00000496437.1:p.Phe63Val
ENST00000646505.1:c.187T>G	ENSP00000496673.1:p.Phe63Val
ENST00000647492.1:c.187T>G	ENSP00000495340.1:p.Phe63Val
ENST00000276110.6:n.572T>G
ENST00000374188.7:c.-530T>G	ENSP00000363303.3:n.-530T>G
ENST00000374202.6:c.187T>G	ENSP00000363318.2:p.Phe63Val
ENST00000456850.6:c.24+446T>G	ENSP00000388967.2:n.24+446T>G
ENST00000464642.5:c.55T>G	ENSP00000425233.1:p.Phe19Val
ENST00000473378.1:c.124T>G	ENSP00000423601.1:p.Phe42Val
ENST00000487883.1:c.151T>G	ENSP00000423966.1:p.Phe51Val
ENST00000512747.3:n.254T>G
NM_000206.2:c.187T>G , LRG_150t1:c.187T>G	NP_000197.1:p.Phe63Val
NM_000206.3:c.187T>G MANE Select	NP_000197.1:p.Phe63Val