Canonical Allele Identifier: CA1888025437
Community Standard Title: NM_000417.3(IL2RA):c.516C= (p.His172=)
Gene: IL2RA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6021545G= , CM000672.2:g.6021545G= GRCh38
NC_000010.10:g.6063508G= , CM000672.1:g.6063508G= GRCh37
NC_000010.9:g.6103514G= NCBI36
NG_007403.1:g.45765C= , LRG_73:g.45765C=

Transcript Alleles

HGVS Amino-acid Change
NM_000417.3:c.516C= MANE Select NP_000408.1:p.His172=
ENST00000379959.8:c.516C= MANE Select ENSP00000369293.3:p.His172=
NM_000417.2:c.516C= , LRG_73t1:c.516C= NP_000408.1:p.His172=
NM_001308242.1:c.368-1604C= NP_001295171.1:n.368-1604C=
NM_001308242.2:c.368-1604C= NP_001295171.1:n.368-1604C=
NM_001308243.1:c.368-2046C= NP_001295172.1:n.368-2046C=
NM_001308243.2:c.368-2046C= NP_001295172.1:n.368-2046C=
ENST00000256876.10:c.516C= ENSP00000256876.6:p.His172=
ENST00000379954.5:c.368-1604C= ENSP00000369287.1:n.368-1604C=
ENST00000379959.7:c.516C= ENSP00000369293.3:p.His172=
ENST00000447847.1:c.280-2046C=
ENST00000447847.2:c.368-2046C= ENSP00000402024.2:n.368-2046C=
ENST00000697424.1:c.516C= ENSP00000513307.1:p.His172=