This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA2436347881
Gene: IL2RG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71108233T= , CM000685.2:g.71108233T= GRCh38
NC_000023.10:g.70328083T= , CM000685.1:g.70328083T= GRCh37
NC_000023.9:g.70244808T= NCBI36
NG_009088.1:g.8321A= , LRG_150:g.8321A=
NG_021141.1:g.3556A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.*44+44A= ENSP00000421262.2:n.*44+44A=
ENST00000696903.1:n.1227+44A=
ENST00000374202.7:c.924+44A= MANE Select ENSP00000363318.3:n.924+44A=
ENST00000642473.1:n.1288+44A=
ENST00000644022.1:n.1190+44A=
ENST00000644708.1:n.1233+44A=
ENST00000644911.1:n.1330+44A=
ENST00000645266.1:c.924+44A= ENSP00000493734.1:n.924+44A=
ENST00000645518.1:c.924+44A= ENSP00000493986.1:n.924+44A=
ENST00000646106.1:c.924+44A= ENSP00000496437.1:n.924+44A=
ENST00000646505.1:c.924+44A= ENSP00000496673.1:n.924+44A=
ENST00000647492.1:c.924+44A= ENSP00000495340.1:n.924+44A=
ENST00000276110.6:n.1517+44A=
ENST00000374188.7:c.111+44A= ENSP00000363303.3:n.111+44A=
ENST00000374202.6:c.924+44A= ENSP00000363318.2:n.924+44A=
ENST00000456850.6:c.354+44A= ENSP00000388967.2:n.354+44A=
ENST00000482750.5:c.240+44A=
ENST00000512747.3:n.1147A=
NM_000206.2:c.924+44A= , LRG_150t1:c.924+44A= NP_000197.1:n.924+44A=
NM_000206.3:c.924+44A= MANE Select NP_000197.1:n.924+44A=
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