Canonical Allele Identifier: CA412245578

Gene: IL3RA

Linked Data

• dbSNP Id: rs1205967577
• gnomAD v2: X-1471047-A-G
• gnomAD v4: X-1352154-A-G
• MyVariant Identifiers: chrX:g.1471047A>G (hg19) ; chrX:g.1352154A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352154A>G , CM000685.2:g.1352154A>G	GRCh38
NC_000023.10:g.1471047A>G , CM000685.1:g.1471047A>G	GRCh37
NC_000023.9:g.1431047A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331035.10:c.353A>G MANE Select	ENSP00000327890.4:p.Asp118Gly
ENST00000331035.9:c.353A>G	ENSP00000327890.4:p.Asp118Gly
ENST00000381469.7:c.119A>G	ENSP00000370878.2:p.Asp40Gly
ENST00000432757.6:c.119A>G	ENSP00000414867.1:p.Asp40Gly
XM_005274431.3:c.353A>G	XP_005274488.1:p.Asp118Gly
XM_005274432.1:c.353A>G	XP_005274489.1:p.Asp118Gly
XR_247285.3:n.870+156T>C
XR_430488.2:n.1194+156T>C
XR_430490.2:n.869+156T>C
XR_951269.1:n.1398+156T>C
XR_951270.1:n.1415+156T>C
XR_951271.1:n.1466+156T>C
XR_951272.1:n.1402+156T>C
XR_951273.1:n.1329+156T>C
XR_951274.1:n.1333+156T>C
XR_951276.1:n.1346+156T>C
XR_951277.1:n.1398+156T>C
XR_951278.1:n.1398+156T>C
XR_951279.1:n.1398+156T>C
XR_951280.1:n.1398+156T>C
XR_951281.1:n.1398+156T>C
XR_951282.1:n.1243+156T>C
XR_951283.1:n.872+156T>C
XM_005274431.5:c.353A>G	XP_005274488.1:p.Asp118Gly
XM_017029491.2:c.353A>G	XP_016884980.1:p.Asp118Gly
XR_001755748.1:n.1189+156T>C
XR_001755751.1:n.1189+156T>C
XR_001755752.1:n.1189+156T>C
XR_001755754.1:n.1189+156T>C