Canonical Allele Identifier: CA515393118

Gene: IL3RA

Linked Data

• dbSNP Id: rs1445376991
• gnomAD v4: X-1352358-G-A
• MyVariant Identifiers: chrX:g.1471251G>A (hg19) ; chrX:g.1352358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352358G>A , CM000685.2:g.1352358G>A	GRCh38
NC_000023.10:g.1471251G>A , CM000685.1:g.1471251G>A	GRCh37
NC_000023.9:g.1431251G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.468G>A MANE Select	ENSP00000327890.4:p.Thr156=
ENST00000331035.9:c.468G>A	ENSP00000327890.4:p.Thr156=
ENST00000381469.7:c.234G>A	ENSP00000370878.2:p.Thr78=
ENST00000432757.6:c.234G>A	ENSP00000414867.1:p.Thr78=
XM_005274431.3:c.468G>A	XP_005274488.1:p.Thr156=
XM_005274432.1:c.465G>A	XP_005274489.1:p.Thr155=
XR_247285.3:n.822C>T
XR_430488.2:n.1146C>T
XR_430490.2:n.821C>T
XR_951269.1:n.1350C>T
XR_951270.1:n.1367C>T
XR_951271.1:n.1418C>T
XR_951272.1:n.1354C>T
XR_951273.1:n.1281C>T
XR_951274.1:n.1285C>T
XR_951276.1:n.1298C>T
XR_951277.1:n.1350C>T
XR_951278.1:n.1350C>T
XR_951279.1:n.1350C>T
XR_951280.1:n.1350C>T
XR_951281.1:n.1350C>T
XR_951282.1:n.1195C>T
XR_951283.1:n.824C>T
XM_005274431.5:c.468G>A	XP_005274488.1:p.Thr156=
XM_017029491.2:c.465G>A	XP_016884980.1:p.Thr155=
XR_001755748.1:n.1141C>T
XR_001755751.1:n.1141C>T
XR_001755752.1:n.1141C>T
XR_001755754.1:n.1141C>T