Canonical Allele Identifier: CA1888011712
Gene: IL2RA HGNC NCBI

Linked Data

dbSNP Id: rs1839182691
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6010939A>G , CM000672.2:g.6010939A>G GRCh38
NC_000010.10:g.6052902A>G , CM000672.1:g.6052902A>G GRCh37
NC_000010.9:g.6092908A>G NCBI36
NG_007403.1:g.56371T>C , LRG_73:g.56371T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379959.8:c.*1933T>C MANE Select ENSP00000369293.3:n.*1933T>C
ENST00000649218.1:n.2567T>C
ENST00000379959.7:c.*1933T>C ENSP00000369293.3:n.*1933T>C
NM_000417.2:c.*1933T>C , LRG_73t1:c.*1933T>C NP_000408.1:n.*1933T>C
NM_001308242.1:c.*1933T>C NP_001295171.1:n.*1933T>C
NM_001308243.1:c.*1933T>C NP_001295172.1:n.*1933T>C
NM_000417.3:c.*1933T>C MANE Select NP_000408.1:n.*1933T>C
NM_001308242.2:c.*1933T>C NP_001295171.1:n.*1933T>C
NM_001308243.2:c.*1933T>C NP_001295172.1:n.*1933T>C
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