Canonical Allele Identifier: CA2721057815

Gene: IL2RA

Linked Data

• dbSNP Id: rs2132908217

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.6059793A>G , CM000672.2:g.6059793A>G	GRCh38
NC_000010.10:g.6101756A>G , CM000672.1:g.6101756A>G	GRCh37
NC_000010.9:g.6141762A>G	NCBI36
NG_007403.1:g.7517T>C , LRG_73:g.7517T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000447847.2:c.64+2295T>C	ENSP00000402024.2:n.64+2295T>C
ENST00000697424.1:c.64+2295T>C	ENSP00000513307.1:n.64+2295T>C
ENST00000379959.8:c.64+2295T>C MANE Select	ENSP00000369293.3:n.64+2295T>C
ENST00000644262.1:n.279+2299T>C
ENST00000256876.10:c.64+2295T>C	ENSP00000256876.6:n.64+2295T>C
ENST00000379954.5:c.64+2295T>C	ENSP00000369287.1:n.64+2295T>C
ENST00000379959.7:c.64+2295T>C	ENSP00000369293.3:n.64+2295T>C
NM_000417.2:c.64+2295T>C , LRG_73t1:c.64+2295T>C	NP_000408.1:n.64+2295T>C
NM_001308242.1:c.64+2295T>C	NP_001295171.1:n.64+2295T>C
NM_001308243.1:c.64+2295T>C	NP_001295172.1:n.64+2295T>C
NM_000417.3:c.64+2295T>C MANE Select	NP_000408.1:n.64+2295T>C
NM_001308242.2:c.64+2295T>C	NP_001295171.1:n.64+2295T>C
NM_001308243.2:c.64+2295T>C	NP_001295172.1:n.64+2295T>C