Canonical Allele Identifier: CA1584711939
Gene: IL9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894864C= , CM000667.2:g.135894864C= GRCh38
NC_000005.9:g.135230553C= , CM000667.1:g.135230553C= GRCh37
NC_000005.8:g.135258452C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.183+576G= MANE Select ENSP00000274520.1:n.183+576G=
ENST00000274520.1:c.183+576G= ENSP00000274520.1:n.183+576G=
NM_000590.1:c.183+576G= NP_000581.1:n.183+576G=
NM_000590.2:c.183+576G= MANE Select NP_000581.1:n.183+576G=
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