Canonical Allele Identifier: CA1584711852
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1762919370
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894759del , CM000667.2:g.135894759del GRCh38
NC_000005.9:g.135230448del , CM000667.1:g.135230448del GRCh37
NC_000005.8:g.135258347del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.184-607del MANE Select ENSP00000274520.1:n.184-607del
ENST00000274520.1:c.184-607del ENSP00000274520.1:n.184-607del
NM_000590.1:c.184-607del NP_000581.1:n.184-607del
NM_000590.2:c.184-607del MANE Select NP_000581.1:n.184-607del
Search 100 bp 5'
Search 100 bp 3'