Canonical Allele Identifier: CA13302800
Gene: IL2RA HGNC NCBI

Linked Data

dbSNP Id: rs4749924
gnomAD v2: 10-6082396-A-C
gnomAD v3: 10-6040433-A-C
gnomAD v4: 10-6040433-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.6040433A>C , CM000672.2:g.6040433A>C GRCh38
NC_000010.10:g.6082396A>C , CM000672.1:g.6082396A>C GRCh37
NC_000010.9:g.6122402A>C NCBI36
NG_007403.1:g.26877T>G , LRG_73:g.26877T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000447847.2:c.65-14408T>G ENSP00000402024.2:n.65-14408T>G
ENST00000697424.1:c.65-14408T>G ENSP00000513307.1:n.65-14408T>G
ENST00000379959.8:c.65-14408T>G MANE Select ENSP00000369293.3:n.65-14408T>G
ENST00000644262.1:n.280-691T>G
ENST00000256876.10:c.65-14408T>G ENSP00000256876.6:n.65-14408T>G
ENST00000379954.5:c.65-14408T>G ENSP00000369287.1:n.65-14408T>G
ENST00000379959.7:c.65-14408T>G ENSP00000369293.3:n.65-14408T>G
NM_000417.2:c.65-14408T>G , LRG_73t1:c.65-14408T>G NP_000408.1:n.65-14408T>G
NM_001308242.1:c.65-14408T>G NP_001295171.1:n.65-14408T>G
NM_001308243.1:c.65-14408T>G NP_001295172.1:n.65-14408T>G
NM_000417.3:c.65-14408T>G MANE Select NP_000408.1:n.65-14408T>G
NM_001308242.2:c.65-14408T>G NP_001295171.1:n.65-14408T>G
NM_001308243.2:c.65-14408T>G NP_001295172.1:n.65-14408T>G