Canonical Allele Identifier: CA1584711858
Gene: IL9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894771_135894772delinsAC , CM000667.2:g.135894771_135894772delinsAC GRCh38
NC_000005.9:g.135230460_135230461delinsAC , CM000667.1:g.135230460_135230461delinsAC GRCh37
NC_000005.8:g.135258359_135258360delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.184-621_184-620delinsGT MANE Select ENSP00000274520.1:n.184-621_184-620delinsGT
ENST00000274520.1:c.184-621_184-620delinsGT ENSP00000274520.1:n.184-621_184-620delinsGT
NM_000590.1:c.184-621_184-620delinsGT NP_000581.1:n.184-621_184-620delinsGT
NM_000590.2:c.184-621_184-620delinsGT MANE Select NP_000581.1:n.184-621_184-620delinsGT