Canonical Allele Identifier: CA2436348267

Gene: IL2RG

Linked Data

• dbSNP Id: rs2092258720

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109561dup , CM000685.2:g.71109561dup	GRCh38
NC_000023.10:g.70329411dup , CM000685.1:g.70329411dup	GRCh37
NC_000023.9:g.70246136dup	NCBI36
NG_009088.1:g.6996dup , LRG_150:g.6996dup
NG_021141.1:g.2231dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.595-168dup	ENSP00000421262.2:n.595-168dup
ENST00000696903.1:n.646-168dup
ENST00000374202.7:c.595-168dup MANE Select	ENSP00000363318.3:n.595-168dup
ENST00000642473.1:n.959-168dup
ENST00000644022.1:n.861-168dup
ENST00000644708.1:n.1001-168dup
ENST00000644911.1:n.1001-168dup
ENST00000645266.1:c.595-168dup	ENSP00000493734.1:n.595-168dup
ENST00000645518.1:c.595-168dup	ENSP00000493986.1:n.595-168dup
ENST00000646106.1:c.595-168dup	ENSP00000496437.1:n.595-168dup
ENST00000646505.1:c.595-168dup	ENSP00000496673.1:n.595-168dup
ENST00000647492.1:c.595-168dup	ENSP00000495340.1:n.595-168dup
ENST00000276110.6:n.1188-168dup
ENST00000374188.7:c.-122-168dup	ENSP00000363303.3:n.-122-168dup
ENST00000374202.6:c.595-168dup	ENSP00000363318.2:n.595-168dup
ENST00000456850.6:c.25-168dup	ENSP00000388967.2:n.25-168dup
ENST00000464642.5:c.463-168dup	ENSP00000425233.1:n.463-168dup
ENST00000482750.5:c.8-168dup
ENST00000512747.3:n.522-168dup
NM_000206.2:c.595-168dup , LRG_150t1:c.595-168dup	NP_000197.1:n.595-168dup
NM_000206.3:c.595-168dup MANE Select	NP_000197.1:n.595-168dup