Canonical Allele Identifier: CA1888011783
Gene: IL2RA HGNC NCBI

Linked Data

dbSNP Id: rs1839184873
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6011117C>T , CM000672.2:g.6011117C>T GRCh38
NC_000010.10:g.6053080C>T , CM000672.1:g.6053080C>T GRCh37
NC_000010.9:g.6093086C>T NCBI36
NG_007403.1:g.56193G>A , LRG_73:g.56193G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379959.8:c.*1755G>A MANE Select ENSP00000369293.3:n.*1755G>A
ENST00000649218.1:n.2389G>A
ENST00000379959.7:c.*1755G>A ENSP00000369293.3:n.*1755G>A
NM_000417.2:c.*1755G>A , LRG_73t1:c.*1755G>A NP_000408.1:n.*1755G>A
NM_001308242.1:c.*1755G>A NP_001295171.1:n.*1755G>A
NM_001308243.1:c.*1755G>A NP_001295172.1:n.*1755G>A
NM_000417.3:c.*1755G>A MANE Select NP_000408.1:n.*1755G>A
NM_001308242.2:c.*1755G>A NP_001295171.1:n.*1755G>A
NM_001308243.2:c.*1755G>A NP_001295172.1:n.*1755G>A
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