Canonical Allele Identifier: CA413497044

Gene: IL2RG

Linked Data

• MyVariant Identifiers: chrX:g.70330785G>T (hg19) ; chrX:g.71110935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71110935G>T , CM000685.2:g.71110935G>T	GRCh38
NC_000023.10:g.70330785G>T , CM000685.1:g.70330785G>T	GRCh37
NC_000023.9:g.70247510G>T	NCBI36
NG_009088.1:g.5619C>A , LRG_150:g.5619C>A
NG_021141.1:g.854C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.231C>A	ENSP00000421262.2:p.Ser77Arg
ENST00000696903.1:n.282C>A
ENST00000374202.7:c.231C>A MANE Select	ENSP00000363318.3:p.Ser77Arg
ENST00000642473.1:n.595C>A
ENST00000644022.1:n.637C>A
ENST00000644708.1:n.637C>A
ENST00000644911.1:n.637C>A
ENST00000645266.1:c.231C>A	ENSP00000493734.1:p.Ser77Arg
ENST00000645518.1:c.231C>A	ENSP00000493986.1:p.Ser77Arg
ENST00000646106.1:c.231C>A	ENSP00000496437.1:p.Ser77Arg
ENST00000646505.1:c.231C>A	ENSP00000496673.1:p.Ser77Arg
ENST00000647492.1:c.231C>A	ENSP00000495340.1:p.Ser77Arg
ENST00000276110.6:n.616C>A
ENST00000374188.7:c.-486C>A	ENSP00000363303.3:n.-486C>A
ENST00000374202.6:c.231C>A	ENSP00000363318.2:p.Ser77Arg
ENST00000456850.6:c.24+490C>A	ENSP00000388967.2:n.24+490C>A
ENST00000464642.5:c.99C>A	ENSP00000425233.1:p.Ser33Arg
ENST00000473378.1:c.168C>A	ENSP00000423601.1:p.Ser56Arg
ENST00000487883.1:c.195C>A	ENSP00000423966.1:p.Ser65Arg
ENST00000512747.3:n.298C>A
NM_000206.2:c.231C>A , LRG_150t1:c.231C>A	NP_000197.1:p.Ser77Arg
NM_000206.3:c.231C>A MANE Select	NP_000197.1:p.Ser77Arg