Canonical Allele Identifier: CA516705753

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70329190C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109340C>G , CM000685.2:g.71109340C>G	GRCh38
NC_000023.10:g.70329190C>G , CM000685.1:g.70329190C>G	GRCh37
NC_000023.9:g.70245915C>G	NCBI36
NG_009088.1:g.7214G>C , LRG_150:g.7214G>C
NG_021141.1:g.2449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.645G>C	ENSP00000421262.2:p.Gly215=
ENST00000696903.1:n.696G>C
ENST00000374202.7:c.645G>C MANE Select	ENSP00000363318.3:p.Gly215=
ENST00000642473.1:n.1009G>C
ENST00000644022.1:n.911G>C
ENST00000644708.1:n.1051G>C
ENST00000644911.1:n.1051G>C
ENST00000645266.1:c.645G>C	ENSP00000493734.1:p.Gly215=
ENST00000645518.1:c.645G>C	ENSP00000493986.1:p.Gly215=
ENST00000646106.1:c.645G>C	ENSP00000496437.1:p.Gly215=
ENST00000646505.1:c.645G>C	ENSP00000496673.1:p.Gly215=
ENST00000647492.1:c.645G>C	ENSP00000495340.1:p.Gly215=
ENST00000276110.6:n.1238G>C
ENST00000374188.7:c.-72G>C	ENSP00000363303.3:n.-72G>C
ENST00000374202.6:c.645G>C	ENSP00000363318.2:p.Gly215=
ENST00000456850.6:c.75G>C	ENSP00000388967.2:p.Gly25=
ENST00000464642.5:c.513G>C	ENSP00000425233.1:p.Gly171=
ENST00000482750.5:c.58G>C
ENST00000512747.3:n.572G>C
NM_000206.2:c.645G>C , LRG_150t1:c.645G>C	NP_000197.1:p.Gly215=
NM_000206.3:c.645G>C MANE Select	NP_000197.1:p.Gly215=