Canonical Allele Identifier: CA14999610
Gene: IL3RA HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1352044C>T , CM000685.2:g.1352044C>T GRCh38
NC_000023.10:g.1470937C>T , CM000685.1:g.1470937C>T GRCh37
NC_000023.9:g.1430937C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331035.10:c.299-56C>T MANE Select ENSP00000327890.4:n.299-56C>T
ENST00000331035.9:c.299-56C>T ENSP00000327890.4:n.299-56C>T
ENST00000381469.7:c.65-56C>T ENSP00000370878.2:n.65-56C>T
ENST00000432757.6:c.65-56C>T ENSP00000414867.1:n.65-56C>T
XM_005274431.3:c.299-56C>T XP_005274488.1:n.299-56C>T
XM_005274432.1:c.299-56C>T XP_005274489.1:n.299-56C>T
XR_247285.3:n.870+266G>A
XR_430488.2:n.1194+266G>A
XR_430490.2:n.869+266G>A
XR_951269.1:n.1398+266G>A
XR_951270.1:n.1415+266G>A
XR_951271.1:n.1466+266G>A
XR_951272.1:n.1402+266G>A
XR_951273.1:n.1329+266G>A
XR_951274.1:n.1333+266G>A
XR_951276.1:n.1346+266G>A
XR_951277.1:n.1398+266G>A
XR_951278.1:n.1398+266G>A
XR_951279.1:n.1398+266G>A
XR_951280.1:n.1398+266G>A
XR_951281.1:n.1398+266G>A
XR_951282.1:n.1243+266G>A
XR_951283.1:n.872+266G>A
XM_005274431.5:c.299-56C>T XP_005274488.1:n.299-56C>T
XM_017029491.2:c.299-56C>T XP_016884980.1:n.299-56C>T
XR_001755748.1:n.1189+266G>A
XR_001755751.1:n.1189+266G>A
XR_001755752.1:n.1189+266G>A
XR_001755754.1:n.1189+266G>A