Canonical Allele Identifier: CA202287777

Gene: IL2RA

Linked Data

• dbSNP Id: rs1042859315
• MyVariant Identifiers: chr10:g.6053173A>T (hg19) ; chr10:g.6011210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6011210A>T , CM000672.2:g.6011210A>T	GRCh38
NC_000010.10:g.6053173A>T , CM000672.1:g.6053173A>T	GRCh37
NC_000010.9:g.6093179A>T	NCBI36
NG_007403.1:g.56100T>A , LRG_73:g.56100T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379959.8:c.*1662T>A MANE Select	ENSP00000369293.3:n.*1662T>A
ENST00000649218.1:n.2296T>A
ENST00000379959.7:c.*1662T>A	ENSP00000369293.3:n.*1662T>A
NM_000417.2:c.*1662T>A , LRG_73t1:c.*1662T>A	NP_000408.1:n.*1662T>A
NM_001308242.1:c.*1662T>A	NP_001295171.1:n.*1662T>A
NM_001308243.1:c.*1662T>A	NP_001295172.1:n.*1662T>A
NM_000417.3:c.*1662T>A MANE Select	NP_000408.1:n.*1662T>A
NM_001308242.2:c.*1662T>A	NP_001295171.1:n.*1662T>A
NM_001308243.2:c.*1662T>A	NP_001295172.1:n.*1662T>A