Canonical Allele Identifier: CA2580908647
Gene: IL2RA HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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