Canonical Allele Identifier: CA254980
Gene: IL2RG HGNC NCBI

Linked Data

ClinVar Variation Id: 10019
ClinVar RCV Id: RCV000010702
dbSNP Id: rs111033619

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.71110980A>T , CM000685.2:g.71110980A>T GRCh38
NC_000023.10:g.70330830A>T , CM000685.1:g.70330830A>T GRCh37
NC_000023.9:g.70247555A>T NCBI36
NG_009088.1:g.5574T>A , LRG_150:g.5574T>A
NG_021141.1:g.809T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000482750.6:c.186T>A ENSP00000421262.2:p.Cys62Ter
ENST00000696903.1:n.237T>A
ENST00000374202.7:c.186T>A MANE Select ENSP00000363318.3:p.Cys62Ter
ENST00000642473.1:n.550T>A
ENST00000644022.1:n.592T>A
ENST00000644708.1:n.592T>A
ENST00000644911.1:n.592T>A
ENST00000645266.1:c.186T>A ENSP00000493734.1:p.Cys62Ter
ENST00000645518.1:c.186T>A ENSP00000493986.1:p.Cys62Ter
ENST00000646106.1:c.186T>A ENSP00000496437.1:p.Cys62Ter
ENST00000646505.1:c.186T>A ENSP00000496673.1:p.Cys62Ter
ENST00000647492.1:c.186T>A ENSP00000495340.1:p.Cys62Ter
ENST00000276110.6:n.571T>A
ENST00000374188.7:c.-531T>A ENSP00000363303.3:n.-531T>A
ENST00000374202.6:c.186T>A ENSP00000363318.2:p.Cys62Ter
ENST00000456850.6:c.24+445T>A ENSP00000388967.2:n.24+445T>A
ENST00000464642.5:c.54T>A ENSP00000425233.1:p.Cys18Ter
ENST00000473378.1:c.123T>A ENSP00000423601.1:p.Cys41Ter
ENST00000487883.1:c.150T>A ENSP00000423966.1:p.Cys50Ter
ENST00000512747.3:n.253T>A
NM_000206.2:c.186T>A , LRG_150t1:c.186T>A NP_000197.1:p.Cys62Ter
NM_000206.3:c.186T>A MANE Select NP_000197.1:p.Cys62Ter