Canonical Allele Identifier: CA202314762

Gene: IL2RA

Linked Data

• dbSNP Id: rs1040754832
• gnomAD v3: 10-6057037-G-T
• gnomAD v4: 10-6057037-G-T
• MyVariant Identifiers: chr10:g.6099000G>T (hg19) ; chr10:g.6057037G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6057037G>T , CM000672.2:g.6057037G>T	GRCh38
NC_000010.10:g.6099000G>T , CM000672.1:g.6099000G>T	GRCh37
NC_000010.9:g.6139006G>T	NCBI36
NG_007403.1:g.10273C>A , LRG_73:g.10273C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447847.2:c.64+5051C>A	ENSP00000402024.2:n.64+5051C>A
ENST00000697424.1:c.64+5051C>A	ENSP00000513307.1:n.64+5051C>A
ENST00000379959.8:c.64+5051C>A MANE Select	ENSP00000369293.3:n.64+5051C>A
ENST00000644262.1:n.279+5055C>A
ENST00000256876.10:c.64+5051C>A	ENSP00000256876.6:n.64+5051C>A
ENST00000379954.5:c.64+5051C>A	ENSP00000369287.1:n.64+5051C>A
ENST00000379959.7:c.64+5051C>A	ENSP00000369293.3:n.64+5051C>A
NM_000417.2:c.64+5051C>A , LRG_73t1:c.64+5051C>A	NP_000408.1:n.64+5051C>A
NM_001308242.1:c.64+5051C>A	NP_001295171.1:n.64+5051C>A
NM_001308243.1:c.64+5051C>A	NP_001295172.1:n.64+5051C>A
NM_000417.3:c.64+5051C>A MANE Select	NP_000408.1:n.64+5051C>A
NM_001308242.2:c.64+5051C>A	NP_001295171.1:n.64+5051C>A
NM_001308243.2:c.64+5051C>A	NP_001295172.1:n.64+5051C>A