Canonical Allele Identifier: CA413497597
Gene: IL2RG HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71111440C>T , CM000685.2:g.71111440C>T GRCh38
NC_000023.10:g.70331290C>T , CM000685.1:g.70331290C>T GRCh37
NC_000023.9:g.70248015C>T NCBI36
NG_009088.1:g.5114G>A , LRG_150:g.5114G>A
NG_021141.1:g.349G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.100G>A ENSP00000421262.2:p.Glu34Lys
ENST00000696903.1:n.151G>A
ENST00000374202.7:c.100G>A MANE Select ENSP00000363318.3:p.Glu34Lys
ENST00000642473.1:n.90G>A
ENST00000644022.1:n.132G>A
ENST00000644708.1:n.132G>A
ENST00000644911.1:n.132G>A
ENST00000645266.1:c.100G>A ENSP00000493734.1:p.Glu34Lys
ENST00000645518.1:c.100G>A ENSP00000493986.1:p.Glu34Lys
ENST00000646106.1:c.100G>A ENSP00000496437.1:p.Glu34Lys
ENST00000646505.1:c.100G>A ENSP00000496673.1:p.Glu34Lys
ENST00000647492.1:c.100G>A ENSP00000495340.1:p.Glu34Lys
ENST00000276110.6:n.111G>A
ENST00000374188.7:c.-617G>A ENSP00000363303.3:n.-617G>A
ENST00000374202.6:c.100G>A ENSP00000363318.2:p.Glu34Lys
ENST00000456850.6:c.9G>A ENSP00000388967.2:p.Met3Ile
ENST00000464642.5:c.-33G>A ENSP00000425233.1:n.-33G>A
ENST00000473378.1:c.9G>A ENSP00000423601.1:p.Met3Ile
ENST00000487883.1:c.-311G>A ENSP00000423966.1:n.-311G>A
ENST00000512747.3:n.167G>A
NM_000206.2:c.100G>A , LRG_150t1:c.100G>A NP_000197.1:p.Glu34Lys
NM_000206.3:c.100G>A MANE Select NP_000197.1:p.Glu34Lys