Canonical Allele Identifier: CA1584711851
Gene: IL9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894757_135894758delinsTC , CM000667.2:g.135894757_135894758delinsTC GRCh38
NC_000005.9:g.135230446_135230447delinsTC , CM000667.1:g.135230446_135230447delinsTC GRCh37
NC_000005.8:g.135258345_135258346delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.184-607_184-606delinsGA MANE Select ENSP00000274520.1:n.184-607_184-606delinsGA
ENST00000274520.1:c.184-607_184-606delinsGA ENSP00000274520.1:n.184-607_184-606delinsGA
NM_000590.1:c.184-607_184-606delinsGA NP_000581.1:n.184-607_184-606delinsGA
NM_000590.2:c.184-607_184-606delinsGA MANE Select NP_000581.1:n.184-607_184-606delinsGA