Canonical Allele Identifier: CA1584711859
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1762919478
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894773del , CM000667.2:g.135894773del GRCh38
NC_000005.9:g.135230462del , CM000667.1:g.135230462del GRCh37
NC_000005.8:g.135258361del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.184-621del MANE Select ENSP00000274520.1:n.184-621del
ENST00000274520.1:c.184-621del ENSP00000274520.1:n.184-621del
NM_000590.1:c.184-621del NP_000581.1:n.184-621del
NM_000590.2:c.184-621del MANE Select NP_000581.1:n.184-621del
Search 100 bp 5'
Search 100 bp 3'