Canonical Allele Identifier: CA2608135135
Gene: IL2RA HGNC NCBI

Linked Data

gnomAD v4: 10-6011231-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6011231A>G , CM000672.2:g.6011231A>G GRCh38
NC_000010.10:g.6053194A>G , CM000672.1:g.6053194A>G GRCh37
NC_000010.9:g.6093200A>G NCBI36
NG_007403.1:g.56079T>C , LRG_73:g.56079T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379959.8:c.*1641T>C MANE Select ENSP00000369293.3:n.*1641T>C
ENST00000649218.1:n.2275T>C
ENST00000379959.7:c.*1641T>C ENSP00000369293.3:n.*1641T>C
NM_000417.2:c.*1641T>C , LRG_73t1:c.*1641T>C NP_000408.1:n.*1641T>C
NM_001308242.1:c.*1641T>C NP_001295171.1:n.*1641T>C
NM_001308243.1:c.*1641T>C NP_001295172.1:n.*1641T>C
NM_000417.3:c.*1641T>C MANE Select NP_000408.1:n.*1641T>C
NM_001308242.2:c.*1641T>C NP_001295171.1:n.*1641T>C
NM_001308243.2:c.*1641T>C NP_001295172.1:n.*1641T>C
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