Canonical Allele Identifier: CA2436348733

Gene: IL2RG

Linked Data

• ClinVar Variation Id: 1561686
• ClinVar RCV Id: RCV002200397
• dbSNP Id: rs2092262251

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110882C>T , CM000685.2:g.71110882C>T	GRCh38
NC_000023.10:g.70330732C>T , CM000685.1:g.70330732C>T	GRCh37
NC_000023.9:g.70247457C>T	NCBI36
NG_009088.1:g.5672G>A , LRG_150:g.5672G>A
NG_021141.1:g.907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.269+15G>A	ENSP00000421262.2:n.269+15G>A
ENST00000696903.1:n.320+15G>A
ENST00000374202.7:c.269+15G>A MANE Select	ENSP00000363318.3:n.269+15G>A
ENST00000642473.1:n.633+15G>A
ENST00000644022.1:n.675+15G>A
ENST00000644708.1:n.675+15G>A
ENST00000644911.1:n.675+15G>A
ENST00000645266.1:c.269+15G>A	ENSP00000493734.1:n.269+15G>A
ENST00000645518.1:c.269+15G>A	ENSP00000493986.1:n.269+15G>A
ENST00000646106.1:c.269+15G>A	ENSP00000496437.1:n.269+15G>A
ENST00000646505.1:c.269+15G>A	ENSP00000496673.1:n.269+15G>A
ENST00000647492.1:c.269+15G>A	ENSP00000495340.1:n.269+15G>A
ENST00000276110.6:n.654+15G>A
ENST00000374188.7:c.-448+15G>A	ENSP00000363303.3:n.-448+15G>A
ENST00000374202.6:c.269+15G>A	ENSP00000363318.2:n.269+15G>A
ENST00000456850.6:c.24+543G>A	ENSP00000388967.2:n.24+543G>A
ENST00000464642.5:c.137+15G>A	ENSP00000425233.1:n.137+15G>A
ENST00000473378.1:c.206+15G>A	ENSP00000423601.1:n.206+15G>A
ENST00000487883.1:c.233+15G>A	ENSP00000423966.1:n.233+15G>A
ENST00000512747.3:n.336+15G>A
NM_000206.2:c.269+15G>A , LRG_150t1:c.269+15G>A	NP_000197.1:n.269+15G>A
NM_000206.3:c.269+15G>A MANE Select	NP_000197.1:n.269+15G>A