Canonical Allele Identifier: CA1584711884
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1259132209
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894804T>A , CM000667.2:g.135894804T>A GRCh38
NC_000005.9:g.135230493T>A , CM000667.1:g.135230493T>A GRCh37
NC_000005.8:g.135258392T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.183+636A>T MANE Select ENSP00000274520.1:n.183+636A>T
ENST00000274520.1:c.183+636A>T ENSP00000274520.1:n.183+636A>T
NM_000590.1:c.183+636A>T NP_000581.1:n.183+636A>T
NM_000590.2:c.183+636A>T MANE Select NP_000581.1:n.183+636A>T
Search 100 bp 5'
Search 100 bp 3'