Canonical Allele Identifier: CA540773193

Gene: IL5RA

Linked Data

• dbSNP Id: rs1288442609
• gnomAD v2: 3-3118537-A-C
• gnomAD v3: 3-3076853-A-C
• gnomAD v4: 3-3076853-A-C
• MyVariant Identifiers: chr3:g.3118537A>C (hg19) ; chr3:g.3076853A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.3076853A>C , CM000665.2:g.3076853A>C	GRCh38
NC_000003.11:g.3118537A>C , CM000665.1:g.3118537A>C	GRCh37
NC_000003.10:g.3093537A>C	NCBI36
NG_029547.1:g.38522T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000446632.7:c.995-226T>G MANE Select	ENSP00000412209.2:n.995-226T>G
ENST00000256452.7:c.995-226T>G	ENSP00000256452.3:n.995-226T>G
ENST00000418488.6:c.710-226T>G	ENSP00000388858.2:n.710-226T>G
ENST00000438560.5:c.995-226T>G	ENSP00000390753.1:n.995-226T>G
ENST00000446632.6:c.995-226T>G	ENSP00000412209.2:n.995-226T>G
NM_000564.4:c.995-226T>G	NP_000555.2:n.995-226T>G
NM_001243099.1:c.995-226T>G	NP_001230028.1:n.995-226T>G
NM_175726.3:c.995-226T>G	NP_783853.1:n.995-226T>G
XM_011533677.1:c.995-226T>G	XP_011531979.1:n.995-226T>G
XM_011533678.1:c.995-226T>G	XP_011531980.1:n.995-226T>G
XM_011533677.2:c.995-226T>G	XP_011531979.1:n.995-226T>G
XM_011533678.2:c.995-226T>G	XP_011531980.1:n.995-226T>G
NM_000564.5:c.995-226T>G	NP_000555.2:n.995-226T>G
NM_001243099.2:c.995-226T>G	NP_001230028.1:n.995-226T>G
NM_175726.4:c.995-226T>G MANE Select	NP_783853.1:n.995-226T>G