Canonical Allele Identifier: CA2436348243
Gene: IL2RG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71109497T= , CM000685.2:g.71109497T= GRCh38
NC_000023.10:g.70329347T= , CM000685.1:g.70329347T= GRCh37
NC_000023.9:g.70246072T= NCBI36
NG_009088.1:g.7057A= , LRG_150:g.7057A=
NG_021141.1:g.2292A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.595-107A= ENSP00000421262.2:n.595-107A=
ENST00000696903.1:n.646-107A=
ENST00000374202.7:c.595-107A= MANE Select ENSP00000363318.3:n.595-107A=
ENST00000642473.1:n.959-107A=
ENST00000644022.1:n.861-107A=
ENST00000644708.1:n.1001-107A=
ENST00000644911.1:n.1001-107A=
ENST00000645266.1:c.595-107A= ENSP00000493734.1:n.595-107A=
ENST00000645518.1:c.595-107A= ENSP00000493986.1:n.595-107A=
ENST00000646106.1:c.595-107A= ENSP00000496437.1:n.595-107A=
ENST00000646505.1:c.595-107A= ENSP00000496673.1:n.595-107A=
ENST00000647492.1:c.595-107A= ENSP00000495340.1:n.595-107A=
ENST00000276110.6:n.1188-107A=
ENST00000374188.7:c.-122-107A= ENSP00000363303.3:n.-122-107A=
ENST00000374202.6:c.595-107A= ENSP00000363318.2:n.595-107A=
ENST00000456850.6:c.25-107A= ENSP00000388967.2:n.25-107A=
ENST00000464642.5:c.463-107A= ENSP00000425233.1:n.463-107A=
ENST00000482750.5:c.8-107A=
ENST00000512747.3:n.522-107A=
NM_000206.2:c.595-107A= , LRG_150t1:c.595-107A= NP_000197.1:n.595-107A=
NM_000206.3:c.595-107A= MANE Select NP_000197.1:n.595-107A=