Canonical Allele Identifier: CA413496982

Gene: IL2RG

Linked Data

• dbSNP Id: rs1312845538
• gnomAD v2: X-70330757-G-T
• MyVariant Identifiers: chrX:g.70330757G>T (hg19) ; chrX:g.71110907G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110907G>T , CM000685.2:g.71110907G>T	GRCh38
NC_000023.10:g.70330757G>T , CM000685.1:g.70330757G>T	GRCh37
NC_000023.9:g.70247482G>T	NCBI36
NG_009088.1:g.5647C>A , LRG_150:g.5647C>A
NG_021141.1:g.882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.259C>A	ENSP00000421262.2:p.Leu87Met
ENST00000696903.1:n.310C>A
ENST00000374202.7:c.259C>A MANE Select	ENSP00000363318.3:p.Leu87Met
ENST00000642473.1:n.623C>A
ENST00000644022.1:n.665C>A
ENST00000644708.1:n.665C>A
ENST00000644911.1:n.665C>A
ENST00000645266.1:c.259C>A	ENSP00000493734.1:p.Leu87Met
ENST00000645518.1:c.259C>A	ENSP00000493986.1:p.Leu87Met
ENST00000646106.1:c.259C>A	ENSP00000496437.1:p.Leu87Met
ENST00000646505.1:c.259C>A	ENSP00000496673.1:p.Leu87Met
ENST00000647492.1:c.259C>A	ENSP00000495340.1:p.Leu87Met
ENST00000276110.6:n.644C>A
ENST00000374188.7:c.-458C>A	ENSP00000363303.3:n.-458C>A
ENST00000374202.6:c.259C>A	ENSP00000363318.2:p.Leu87Met
ENST00000456850.6:c.24+518C>A	ENSP00000388967.2:n.24+518C>A
ENST00000464642.5:c.127C>A	ENSP00000425233.1:p.Leu43Met
ENST00000473378.1:c.196C>A	ENSP00000423601.1:p.Leu66Met
ENST00000487883.1:c.223C>A	ENSP00000423966.1:p.Leu75Met
ENST00000512747.3:n.326C>A
NM_000206.2:c.259C>A , LRG_150t1:c.259C>A	NP_000197.1:p.Leu87Met
NM_000206.3:c.259C>A MANE Select	NP_000197.1:p.Leu87Met