Canonical Allele Identifier: CA413497030

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330779C>G (hg19) ; chrX:g.71110929C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110929C>G , CM000685.2:g.71110929C>G	GRCh38
NC_000023.10:g.70330779C>G , CM000685.1:g.70330779C>G	GRCh37
NC_000023.9:g.70247504C>G	NCBI36
NG_009088.1:g.5625G>C , LRG_150:g.5625G>C
NG_021141.1:g.860G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.237G>C	ENSP00000421262.2:p.Glu79Asp
ENST00000696903.1:n.288G>C
ENST00000374202.7:c.237G>C MANE Select	ENSP00000363318.3:p.Glu79Asp
ENST00000642473.1:n.601G>C
ENST00000644022.1:n.643G>C
ENST00000644708.1:n.643G>C
ENST00000644911.1:n.643G>C
ENST00000645266.1:c.237G>C	ENSP00000493734.1:p.Glu79Asp
ENST00000645518.1:c.237G>C	ENSP00000493986.1:p.Glu79Asp
ENST00000646106.1:c.237G>C	ENSP00000496437.1:p.Glu79Asp
ENST00000646505.1:c.237G>C	ENSP00000496673.1:p.Glu79Asp
ENST00000647492.1:c.237G>C	ENSP00000495340.1:p.Glu79Asp
ENST00000276110.6:n.622G>C
ENST00000374188.7:c.-480G>C	ENSP00000363303.3:n.-480G>C
ENST00000374202.6:c.237G>C	ENSP00000363318.2:p.Glu79Asp
ENST00000456850.6:c.24+496G>C	ENSP00000388967.2:n.24+496G>C
ENST00000464642.5:c.105G>C	ENSP00000425233.1:p.Glu35Asp
ENST00000473378.1:c.174G>C	ENSP00000423601.1:p.Glu58Asp
ENST00000487883.1:c.201G>C	ENSP00000423966.1:p.Glu67Asp
ENST00000512747.3:n.304G>C
NM_000206.2:c.237G>C , LRG_150t1:c.237G>C	NP_000197.1:p.Glu79Asp
NM_000206.3:c.237G>C MANE Select	NP_000197.1:p.Glu79Asp