Canonical Allele Identifier: CA413497087

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330802A>G (hg19) ; chrX:g.71110952A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110952A>G , CM000685.2:g.71110952A>G	GRCh38
NC_000023.10:g.70330802A>G , CM000685.1:g.70330802A>G	GRCh37
NC_000023.9:g.70247527A>G	NCBI36
NG_009088.1:g.5602T>C , LRG_150:g.5602T>C
NG_021141.1:g.837T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.214T>C	ENSP00000421262.2:p.Cys72Arg
ENST00000696903.1:n.265T>C
ENST00000374202.7:c.214T>C MANE Select	ENSP00000363318.3:p.Cys72Arg
ENST00000642473.1:n.578T>C
ENST00000644022.1:n.620T>C
ENST00000644708.1:n.620T>C
ENST00000644911.1:n.620T>C
ENST00000645266.1:c.214T>C	ENSP00000493734.1:p.Cys72Arg
ENST00000645518.1:c.214T>C	ENSP00000493986.1:p.Cys72Arg
ENST00000646106.1:c.214T>C	ENSP00000496437.1:p.Cys72Arg
ENST00000646505.1:c.214T>C	ENSP00000496673.1:p.Cys72Arg
ENST00000647492.1:c.214T>C	ENSP00000495340.1:p.Cys72Arg
ENST00000276110.6:n.599T>C
ENST00000374188.7:c.-503T>C	ENSP00000363303.3:n.-503T>C
ENST00000374202.6:c.214T>C	ENSP00000363318.2:p.Cys72Arg
ENST00000456850.6:c.24+473T>C	ENSP00000388967.2:n.24+473T>C
ENST00000464642.5:c.82T>C	ENSP00000425233.1:p.Cys28Arg
ENST00000473378.1:c.151T>C	ENSP00000423601.1:p.Cys51Arg
ENST00000487883.1:c.178T>C	ENSP00000423966.1:p.Cys60Arg
ENST00000512747.3:n.281T>C
NM_000206.2:c.214T>C , LRG_150t1:c.214T>C	NP_000197.1:p.Cys72Arg
NM_000206.3:c.214T>C MANE Select	NP_000197.1:p.Cys72Arg