Canonical Allele Identifier: CA413628240

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70328134T>G (hg19) ; chrX:g.71108284T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71108284T>G , CM000685.2:g.71108284T>G	GRCh38
NC_000023.10:g.70328134T>G , CM000685.1:g.70328134T>G	GRCh37
NC_000023.9:g.70244859T>G	NCBI36
NG_009088.1:g.8270A>C , LRG_150:g.8270A>C
NG_021141.1:g.3505A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.*37A>C	ENSP00000421262.2:n.*37A>C
ENST00000696903.1:n.1220A>C
ENST00000374202.7:c.917A>C MANE Select	ENSP00000363318.3:p.Asn306Thr
ENST00000642473.1:n.1281A>C
ENST00000644022.1:n.1183A>C
ENST00000644708.1:n.1226A>C
ENST00000644911.1:n.1323A>C
ENST00000645266.1:c.917A>C	ENSP00000493734.1:p.Asn306Thr
ENST00000645518.1:c.917A>C	ENSP00000493986.1:p.Asn306Thr
ENST00000646106.1:c.917A>C	ENSP00000496437.1:p.Asn306Thr
ENST00000646505.1:c.917A>C	ENSP00000496673.1:p.Asn306Thr
ENST00000647492.1:c.917A>C	ENSP00000495340.1:p.Asn306Thr
ENST00000276110.6:n.1510A>C
ENST00000374188.7:c.104A>C	ENSP00000363303.3:p.Asn35Thr
ENST00000374202.6:c.917A>C	ENSP00000363318.2:p.Asn306Thr
ENST00000456850.6:c.347A>C	ENSP00000388967.2:p.Asn116Thr
ENST00000482750.5:c.233A>C
ENST00000512747.3:n.1096A>C
NM_000206.2:c.917A>C , LRG_150t1:c.917A>C	NP_000197.1:p.Asn306Thr
NM_000206.3:c.917A>C MANE Select	NP_000197.1:p.Asn306Thr