Canonical Allele Identifier: CA2436348700
Gene: IL2RG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110784T= , CM000685.2:g.71110784T= GRCh38
NC_000023.10:g.70330634T= , CM000685.1:g.70330634T= GRCh37
NC_000023.9:g.70247359T= NCBI36
NG_009088.1:g.5770A= , LRG_150:g.5770A=
NG_021141.1:g.1005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.270-96A= ENSP00000421262.2:n.270-96A=
ENST00000696903.1:n.321-96A=
ENST00000374202.7:c.270-96A= MANE Select ENSP00000363318.3:n.270-96A=
ENST00000642473.1:n.634-96A=
ENST00000644022.1:n.676-96A=
ENST00000644708.1:n.676-96A=
ENST00000644911.1:n.676-96A=
ENST00000645266.1:c.270-96A= ENSP00000493734.1:n.270-96A=
ENST00000645518.1:c.270-96A= ENSP00000493986.1:n.270-96A=
ENST00000646106.1:c.270-96A= ENSP00000496437.1:n.270-96A=
ENST00000646505.1:c.270-96A= ENSP00000496673.1:n.270-96A=
ENST00000647492.1:c.270-96A= ENSP00000495340.1:n.270-96A=
ENST00000276110.6:n.655-96A=
ENST00000374188.7:c.-447-96A= ENSP00000363303.3:n.-447-96A=
ENST00000374202.6:c.270-96A= ENSP00000363318.2:n.270-96A=
ENST00000456850.6:c.24+641A= ENSP00000388967.2:n.24+641A=
ENST00000464642.5:c.138-96A= ENSP00000425233.1:n.138-96A=
ENST00000473378.1:c.207-96A= ENSP00000423601.1:n.207-96A=
ENST00000487883.1:c.234-96A= ENSP00000423966.1:n.234-96A=
ENST00000512747.3:n.337-96A=
NM_000206.2:c.270-96A= , LRG_150t1:c.270-96A= NP_000197.1:n.270-96A=
NM_000206.3:c.270-96A= MANE Select NP_000197.1:n.270-96A=