Canonical Allele Identifier: CA1888025493
Community Standard Title: NM_000417.3(IL2RA):c.497G= (p.Ser166=)
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6021564C= , CM000672.2:g.6021564C= GRCh38
NC_000010.10:g.6063527C= , CM000672.1:g.6063527C= GRCh37
NC_000010.9:g.6103533C= NCBI36
NG_007403.1:g.45746G= , LRG_73:g.45746G=

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.497G= MANE Select NP_000408.1:p.Ser166=
ENST00000379959.8:c.497G= MANE Select ENSP00000369293.3:p.Ser166=
NM_000417.2:c.497G= , LRG_73t1:c.497G= NP_000408.1:p.Ser166=
NM_001308242.1:c.368-1623G= NP_001295171.1:n.368-1623G=
NM_001308242.2:c.368-1623G= NP_001295171.1:n.368-1623G=
NM_001308243.1:c.368-2065G= NP_001295172.1:n.368-2065G=
NM_001308243.2:c.368-2065G= NP_001295172.1:n.368-2065G=
ENST00000256876.10:c.497G= ENSP00000256876.6:p.Ser166=
ENST00000379954.5:c.368-1623G= ENSP00000369287.1:n.368-1623G=
ENST00000379959.7:c.497G= ENSP00000369293.3:p.Ser166=
ENST00000447847.1:c.280-2065G=
ENST00000447847.2:c.368-2065G= ENSP00000402024.2:n.368-2065G=
ENST00000697424.1:c.497G= ENSP00000513307.1:p.Ser166=