Canonical Allele Identifier: CA412245613

Gene: IL3RA

Linked Data

• dbSNP Id: rs2086118227
• MyVariant Identifiers: chrX:g.1471061A>C (hg19) ; chrX:g.1352168A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352168A>C , CM000685.2:g.1352168A>C	GRCh38
NC_000023.10:g.1471061A>C , CM000685.1:g.1471061A>C	GRCh37
NC_000023.9:g.1431061A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.367A>C MANE Select	ENSP00000327890.4:p.Ser123Arg
ENST00000331035.9:c.367A>C	ENSP00000327890.4:p.Ser123Arg
ENST00000381469.7:c.133A>C	ENSP00000370878.2:p.Ser45Arg
ENST00000432757.6:c.133A>C	ENSP00000414867.1:p.Ser45Arg
XM_005274431.3:c.367A>C	XP_005274488.1:p.Ser123Arg
XM_005274432.1:c.367A>C	XP_005274489.1:p.Ser123Arg
XR_247285.3:n.870+142T>G
XR_430488.2:n.1194+142T>G
XR_430490.2:n.869+142T>G
XR_951269.1:n.1398+142T>G
XR_951270.1:n.1415+142T>G
XR_951271.1:n.1466+142T>G
XR_951272.1:n.1402+142T>G
XR_951273.1:n.1329+142T>G
XR_951274.1:n.1333+142T>G
XR_951276.1:n.1346+142T>G
XR_951277.1:n.1398+142T>G
XR_951278.1:n.1398+142T>G
XR_951279.1:n.1398+142T>G
XR_951280.1:n.1398+142T>G
XR_951281.1:n.1398+142T>G
XR_951282.1:n.1243+142T>G
XR_951283.1:n.872+142T>G
XM_005274431.5:c.367A>C	XP_005274488.1:p.Ser123Arg
XM_017029491.2:c.367A>C	XP_016884980.1:p.Ser123Arg
XR_001755748.1:n.1189+142T>G
XR_001755751.1:n.1189+142T>G
XR_001755752.1:n.1189+142T>G
XR_001755754.1:n.1189+142T>G