Canonical Allele Identifier: CA413496166

Gene: IL2RG

Linked Data

• gnomAD v4: X-71109387-G-C
• MyVariant Identifiers: chrX:g.70329237G>C (hg19) ; chrX:g.71109387G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109387G>C , CM000685.2:g.71109387G>C	GRCh38
NC_000023.10:g.70329237G>C , CM000685.1:g.70329237G>C	GRCh37
NC_000023.9:g.70245962G>C	NCBI36
NG_009088.1:g.7167C>G , LRG_150:g.7167C>G
NG_021141.1:g.2402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.598C>G	ENSP00000421262.2:p.Gln200Glu
ENST00000696903.1:n.649C>G
ENST00000374202.7:c.598C>G MANE Select	ENSP00000363318.3:p.Gln200Glu
ENST00000642473.1:n.962C>G
ENST00000644022.1:n.864C>G
ENST00000644708.1:n.1004C>G
ENST00000644911.1:n.1004C>G
ENST00000645266.1:c.598C>G	ENSP00000493734.1:p.Gln200Glu
ENST00000645518.1:c.598C>G	ENSP00000493986.1:p.Gln200Glu
ENST00000646106.1:c.598C>G	ENSP00000496437.1:p.Gln200Glu
ENST00000646505.1:c.598C>G	ENSP00000496673.1:p.Gln200Glu
ENST00000647492.1:c.598C>G	ENSP00000495340.1:p.Gln200Glu
ENST00000276110.6:n.1191C>G
ENST00000374188.7:c.-119C>G	ENSP00000363303.3:n.-119C>G
ENST00000374202.6:c.598C>G	ENSP00000363318.2:p.Gln200Glu
ENST00000456850.6:c.28C>G	ENSP00000388967.2:p.Gln10Glu
ENST00000464642.5:c.466C>G	ENSP00000425233.1:p.Gln156Glu
ENST00000482750.5:c.11C>G
ENST00000512747.3:n.525C>G
NM_000206.2:c.598C>G , LRG_150t1:c.598C>G	NP_000197.1:p.Gln200Glu
NM_000206.3:c.598C>G MANE Select	NP_000197.1:p.Gln200Glu