Canonical Allele Identifier: CA516772439

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70328505A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71108655A>C , CM000685.2:g.71108655A>C	GRCh38
NC_000023.10:g.70328505A>C , CM000685.1:g.70328505A>C	GRCh37
NC_000023.9:g.70245230A>C	NCBI36
NG_009088.1:g.7899T>G , LRG_150:g.7899T>G
NG_021141.1:g.3134T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.758-309T>G	ENSP00000421262.2:n.758-309T>G
ENST00000696903.1:n.849T>G
ENST00000374202.7:c.798T>G MANE Select	ENSP00000363318.3:p.Ser266=
ENST00000642473.1:n.1162T>G
ENST00000644022.1:n.1064T>G
ENST00000644708.1:n.1164-309T>G
ENST00000644911.1:n.1204T>G
ENST00000645266.1:c.798T>G	ENSP00000493734.1:p.Ser266=
ENST00000645518.1:c.798T>G	ENSP00000493986.1:p.Ser266=
ENST00000646106.1:c.798T>G	ENSP00000496437.1:p.Ser266=
ENST00000646505.1:c.798T>G	ENSP00000496673.1:p.Ser266=
ENST00000647492.1:c.798T>G	ENSP00000495340.1:p.Ser266=
ENST00000276110.6:n.1391T>G
ENST00000374188.7:c.42-309T>G	ENSP00000363303.3:n.42-309T>G
ENST00000374202.6:c.798T>G	ENSP00000363318.2:p.Ser266=
ENST00000456850.6:c.228T>G	ENSP00000388967.2:p.Ser76=
ENST00000482750.5:c.171-309T>G
ENST00000512747.3:n.725T>G
NM_000206.2:c.798T>G , LRG_150t1:c.798T>G	NP_000197.1:p.Ser266=
NM_000206.3:c.798T>G MANE Select	NP_000197.1:p.Ser266=