Canonical Allele Identifier: CA1134080417

Gene: IL2RG

Linked Data

• dbSNP Id: rs2092258664
• gnomAD v3: X-71109546-A-AG
• gnomAD v4: X-71109546-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109546_71109547insG , CM000685.2:g.71109546_71109547insG	GRCh38
NC_000023.10:g.70329396_70329397insG , CM000685.1:g.70329396_70329397insG	GRCh37
NC_000023.9:g.70246121_70246122insG	NCBI36
NG_009088.1:g.7007_7008insC , LRG_150:g.7007_7008insC
NG_021141.1:g.2242_2243insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.595-157_595-156insC	ENSP00000421262.2:n.595-157_595-156insC
ENST00000696903.1:n.646-157_646-156insC
ENST00000374202.7:c.595-157_595-156insC MANE Select	ENSP00000363318.3:n.595-157_595-156insC
ENST00000642473.1:n.959-157_959-156insC
ENST00000644022.1:n.861-157_861-156insC
ENST00000644708.1:n.1001-157_1001-156insC
ENST00000644911.1:n.1001-157_1001-156insC
ENST00000645266.1:c.595-157_595-156insC	ENSP00000493734.1:n.595-157_595-156insC
ENST00000645518.1:c.595-157_595-156insC	ENSP00000493986.1:n.595-157_595-156insC
ENST00000646106.1:c.595-157_595-156insC	ENSP00000496437.1:n.595-157_595-156insC
ENST00000646505.1:c.595-157_595-156insC	ENSP00000496673.1:n.595-157_595-156insC
ENST00000647492.1:c.595-157_595-156insC	ENSP00000495340.1:n.595-157_595-156insC
ENST00000276110.6:n.1188-157_1188-156insC
ENST00000374188.7:c.-122-157_-122-156insC	ENSP00000363303.3:n.-122-157_-122-156insC
ENST00000374202.6:c.595-157_595-156insC	ENSP00000363318.2:n.595-157_595-156insC
ENST00000456850.6:c.25-157_25-156insC	ENSP00000388967.2:n.25-157_25-156insC
ENST00000464642.5:c.463-157_463-156insC	ENSP00000425233.1:n.463-157_463-156insC
ENST00000482750.5:c.8-157_8-156insC
ENST00000512747.3:n.522-157_522-156insC
NM_000206.2:c.595-157_595-156insC , LRG_150t1:c.595-157_595-156insC	NP_000197.1:n.595-157_595-156insC
NM_000206.3:c.595-157_595-156insC MANE Select	NP_000197.1:n.595-157_595-156insC