Canonical Allele Identifier: CA516771387
Gene: IL2RG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.70328136C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71108286C>A , CM000685.2:g.71108286C>A GRCh38
NC_000023.10:g.70328136C>A , CM000685.1:g.70328136C>A GRCh37
NC_000023.9:g.70244861C>A NCBI36
NG_009088.1:g.8268G>T , LRG_150:g.8268G>T
NG_021141.1:g.3503G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.*35G>T ENSP00000421262.2:n.*35G>T
ENST00000696903.1:n.1218G>T
ENST00000374202.7:c.915G>T MANE Select ENSP00000363318.3:p.Gly305=
ENST00000642473.1:n.1279G>T
ENST00000644022.1:n.1181G>T
ENST00000644708.1:n.1224G>T
ENST00000644911.1:n.1321G>T
ENST00000645266.1:c.915G>T ENSP00000493734.1:p.Gly305=
ENST00000645518.1:c.915G>T ENSP00000493986.1:p.Gly305=
ENST00000646106.1:c.915G>T ENSP00000496437.1:p.Gly305=
ENST00000646505.1:c.915G>T ENSP00000496673.1:p.Gly305=
ENST00000647492.1:c.915G>T ENSP00000495340.1:p.Gly305=
ENST00000276110.6:n.1508G>T
ENST00000374188.7:c.102G>T ENSP00000363303.3:p.Gly34=
ENST00000374202.6:c.915G>T ENSP00000363318.2:p.Gly305=
ENST00000456850.6:c.345G>T ENSP00000388967.2:p.Gly115=
ENST00000482750.5:c.231G>T
ENST00000512747.3:n.1094G>T
NM_000206.2:c.915G>T , LRG_150t1:c.915G>T NP_000197.1:p.Gly305=
NM_000206.3:c.915G>T MANE Select NP_000197.1:p.Gly305=