Canonical Allele Identifier: CA640360325

Gene: IL3RA

Linked Data

• dbSNP Id: rs1425479598
• gnomAD v2: X-1471182-G-C
• gnomAD v3: X-1352289-G-C
• gnomAD v4: X-1352289-G-C
• MyVariant Identifiers: chrX:g.1471182G>C (hg19) ; chrX:g.1352289G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1352289G>C , CM000685.2:g.1352289G>C	GRCh38
NC_000023.10:g.1471182G>C , CM000685.1:g.1471182G>C	GRCh37
NC_000023.9:g.1431182G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331035.10:c.432-33G>C MANE Select	ENSP00000327890.4:n.432-33G>C
ENST00000331035.9:c.432-33G>C	ENSP00000327890.4:n.432-33G>C
ENST00000381469.7:c.198-33G>C	ENSP00000370878.2:n.198-33G>C
ENST00000432757.6:c.198-33G>C	ENSP00000414867.1:n.198-33G>C
XM_005274431.3:c.432-33G>C	XP_005274488.1:n.432-33G>C
XM_005274432.1:c.432-36G>C	XP_005274489.1:n.432-36G>C
XR_247285.3:n.870+21C>G
XR_430488.2:n.1194+21C>G
XR_430490.2:n.869+21C>G
XR_951269.1:n.1398+21C>G
XR_951270.1:n.1415+21C>G
XR_951271.1:n.1466+21C>G
XR_951272.1:n.1402+21C>G
XR_951273.1:n.1329+21C>G
XR_951274.1:n.1333+21C>G
XR_951276.1:n.1346+21C>G
XR_951277.1:n.1398+21C>G
XR_951278.1:n.1398+21C>G
XR_951279.1:n.1398+21C>G
XR_951280.1:n.1398+21C>G
XR_951281.1:n.1398+21C>G
XR_951282.1:n.1243+21C>G
XR_951283.1:n.872+21C>G
XM_005274431.5:c.432-33G>C	XP_005274488.1:n.432-33G>C
XM_017029491.2:c.432-36G>C	XP_016884980.1:n.432-36G>C
XR_001755748.1:n.1189+21C>G
XR_001755751.1:n.1189+21C>G
XR_001755752.1:n.1189+21C>G
XR_001755754.1:n.1189+21C>G