Canonical Allele Identifier: CA10628718
Gene: IL2RA HGNC NCBI

Linked Data

ClinVar Variation Id: 300218
ClinVar RCV Id: RCV000320848
dbSNP Id: rs12722605
gnomAD v2: 10-6053163-T-A
gnomAD v3: 10-6011200-T-A
gnomAD v4: 10-6011200-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6011200T>A , CM000672.2:g.6011200T>A GRCh38
NC_000010.10:g.6053163T>A , CM000672.1:g.6053163T>A GRCh37
NC_000010.9:g.6093169T>A NCBI36
NG_007403.1:g.56110A>T , LRG_73:g.56110A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379959.8:c.*1672A>T MANE Select ENSP00000369293.3:n.*1672A>T
ENST00000649218.1:n.2306A>T
ENST00000379959.7:c.*1672A>T ENSP00000369293.3:n.*1672A>T
NM_000417.2:c.*1672A>T , LRG_73t1:c.*1672A>T NP_000408.1:n.*1672A>T
NM_001308242.1:c.*1672A>T NP_001295171.1:n.*1672A>T
NM_001308243.1:c.*1672A>T NP_001295172.1:n.*1672A>T
NM_000417.3:c.*1672A>T MANE Select NP_000408.1:n.*1672A>T
NM_001308242.2:c.*1672A>T NP_001295171.1:n.*1672A>T
NM_001308243.2:c.*1672A>T NP_001295172.1:n.*1672A>T