Canonical Allele Identifier: CA1584711900
Gene: IL9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894824G= , CM000667.2:g.135894824G= GRCh38
NC_000005.9:g.135230513G= , CM000667.1:g.135230513G= GRCh37
NC_000005.8:g.135258412G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.183+616C= MANE Select ENSP00000274520.1:n.183+616C=
ENST00000274520.1:c.183+616C= ENSP00000274520.1:n.183+616C=
NM_000590.1:c.183+616C= NP_000581.1:n.183+616C=
NM_000590.2:c.183+616C= MANE Select NP_000581.1:n.183+616C=
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