Canonical Allele Identifier: CA515392911

Gene: IL3RA

Linked Data

• dbSNP Id: rs2086117751
• MyVariant Identifiers: chrX:g.1471052T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352159T>C , CM000685.2:g.1352159T>C	GRCh38
NC_000023.10:g.1471052T>C , CM000685.1:g.1471052T>C	GRCh37
NC_000023.9:g.1431052T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000331035.10:c.358T>C MANE Select	ENSP00000327890.4:p.Leu120=
ENST00000331035.9:c.358T>C	ENSP00000327890.4:p.Leu120=
ENST00000381469.7:c.124T>C	ENSP00000370878.2:p.Leu42=
ENST00000432757.6:c.124T>C	ENSP00000414867.1:p.Leu42=
XM_005274431.3:c.358T>C	XP_005274488.1:p.Leu120=
XM_005274432.1:c.358T>C	XP_005274489.1:p.Leu120=
XR_247285.3:n.870+151A>G
XR_430488.2:n.1194+151A>G
XR_430490.2:n.869+151A>G
XR_951269.1:n.1398+151A>G
XR_951270.1:n.1415+151A>G
XR_951271.1:n.1466+151A>G
XR_951272.1:n.1402+151A>G
XR_951273.1:n.1329+151A>G
XR_951274.1:n.1333+151A>G
XR_951276.1:n.1346+151A>G
XR_951277.1:n.1398+151A>G
XR_951278.1:n.1398+151A>G
XR_951279.1:n.1398+151A>G
XR_951280.1:n.1398+151A>G
XR_951281.1:n.1398+151A>G
XR_951282.1:n.1243+151A>G
XR_951283.1:n.872+151A>G
XM_005274431.5:c.358T>C	XP_005274488.1:p.Leu120=
XM_017029491.2:c.358T>C	XP_016884980.1:p.Leu120=
XR_001755748.1:n.1189+151A>G
XR_001755751.1:n.1189+151A>G
XR_001755752.1:n.1189+151A>G
XR_001755754.1:n.1189+151A>G