Canonical Allele Identifier: CA413496134

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70329223A>C (hg19) ; chrX:g.71109373A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109373A>C , CM000685.2:g.71109373A>C	GRCh38
NC_000023.10:g.70329223A>C , CM000685.1:g.70329223A>C	GRCh37
NC_000023.9:g.70245948A>C	NCBI36
NG_009088.1:g.7181T>G , LRG_150:g.7181T>G
NG_021141.1:g.2416T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.612T>G	ENSP00000421262.2:p.Tyr204Ter
ENST00000696903.1:n.663T>G
ENST00000374202.7:c.612T>G MANE Select	ENSP00000363318.3:p.Tyr204Ter
ENST00000642473.1:n.976T>G
ENST00000644022.1:n.878T>G
ENST00000644708.1:n.1018T>G
ENST00000644911.1:n.1018T>G
ENST00000645266.1:c.612T>G	ENSP00000493734.1:p.Tyr204Ter
ENST00000645518.1:c.612T>G	ENSP00000493986.1:p.Tyr204Ter
ENST00000646106.1:c.612T>G	ENSP00000496437.1:p.Tyr204Ter
ENST00000646505.1:c.612T>G	ENSP00000496673.1:p.Tyr204Ter
ENST00000647492.1:c.612T>G	ENSP00000495340.1:p.Tyr204Ter
ENST00000276110.6:n.1205T>G
ENST00000374188.7:c.-105T>G	ENSP00000363303.3:n.-105T>G
ENST00000374202.6:c.612T>G	ENSP00000363318.2:p.Tyr204Ter
ENST00000456850.6:c.42T>G	ENSP00000388967.2:p.Tyr14Ter
ENST00000464642.5:c.480T>G	ENSP00000425233.1:p.Tyr160Ter
ENST00000482750.5:c.25T>G
ENST00000512747.3:n.539T>G
NM_000206.2:c.612T>G , LRG_150t1:c.612T>G	NP_000197.1:p.Tyr204Ter
NM_000206.3:c.612T>G MANE Select	NP_000197.1:p.Tyr204Ter