Canonical Allele Identifier: CA2436348153

Gene: IL2RG

Linked Data

• dbSNP Id: rs2092257886

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71109180A>G , CM000685.2:g.71109180A>G	GRCh38
NC_000023.10:g.70329030A>G , CM000685.1:g.70329030A>G	GRCh37
NC_000023.9:g.70245755A>G	NCBI36
NG_009088.1:g.7374T>C , LRG_150:g.7374T>C
NG_021141.1:g.2609T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482750.6:c.757+48T>C	ENSP00000421262.2:n.757+48T>C
ENST00000696903.1:n.808+48T>C
ENST00000374202.7:c.757+48T>C MANE Select	ENSP00000363318.3:n.757+48T>C
ENST00000642473.1:n.1121+48T>C
ENST00000644022.1:n.1023+48T>C
ENST00000644708.1:n.1163+48T>C
ENST00000644911.1:n.1163+48T>C
ENST00000645266.1:c.757+48T>C	ENSP00000493734.1:n.757+48T>C
ENST00000645518.1:c.757+48T>C	ENSP00000493986.1:n.757+48T>C
ENST00000646106.1:c.757+48T>C	ENSP00000496437.1:n.757+48T>C
ENST00000646505.1:c.757+48T>C	ENSP00000496673.1:n.757+48T>C
ENST00000647492.1:c.757+48T>C	ENSP00000495340.1:n.757+48T>C
ENST00000276110.6:n.1350+48T>C
ENST00000374188.7:c.41+48T>C	ENSP00000363303.3:n.41+48T>C
ENST00000374202.6:c.757+48T>C	ENSP00000363318.2:n.757+48T>C
ENST00000456850.6:c.187+48T>C	ENSP00000388967.2:n.187+48T>C
ENST00000464642.5:c.625+48T>C	ENSP00000425233.1:n.625+48T>C
ENST00000482750.5:c.170+48T>C
ENST00000512747.3:n.684+48T>C
NM_000206.2:c.757+48T>C , LRG_150t1:c.757+48T>C	NP_000197.1:n.757+48T>C
NM_000206.3:c.757+48T>C MANE Select	NP_000197.1:n.757+48T>C