Canonical Allele Identifier: CA2436348604
Gene: IL2RG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110524A= , CM000685.2:g.71110524A= GRCh38
NC_000023.10:g.70330374A= , CM000685.1:g.70330374A= GRCh37
NC_000023.9:g.70247099A= NCBI36
NG_009088.1:g.6030T= , LRG_150:g.6030T=
NG_021141.1:g.1265T=

Transcript Alleles

HGVS Amino-acid change
ENST00000482750.6:c.434T= ENSP00000421262.2:p.Met145=
ENST00000696903.1:n.485T=
ENST00000374202.7:c.434T= MANE Select ENSP00000363318.3:p.Met145=
ENST00000642473.1:n.798T=
ENST00000644022.1:n.840T=
ENST00000644708.1:n.840T=
ENST00000644911.1:n.840T=
ENST00000645266.1:c.434T= ENSP00000493734.1:p.Met145=
ENST00000645518.1:c.434T= ENSP00000493986.1:p.Met145=
ENST00000646106.1:c.434T= ENSP00000496437.1:p.Met145=
ENST00000646505.1:c.434T= ENSP00000496673.1:p.Met145=
ENST00000647492.1:c.434T= ENSP00000495340.1:p.Met145=
ENST00000276110.6:n.819T=
ENST00000374188.7:c.-283T= ENSP00000363303.3:n.-283T=
ENST00000374202.6:c.434T= ENSP00000363318.2:p.Met145=
ENST00000456850.6:c.24+901T= ENSP00000388967.2:n.24+901T=
ENST00000464642.5:c.302T= ENSP00000425233.1:p.Met101=
ENST00000487883.1:c.398T= ENSP00000423966.1:p.Met133=
ENST00000512747.3:n.501T=
NM_000206.2:c.434T= , LRG_150t1:c.434T= NP_000197.1:p.Met145=
NM_000206.3:c.434T= MANE Select NP_000197.1:p.Met145=