Canonical Allele Identifier: CA1081864432
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1762921188
gnomAD v3: 5-135894973-G-A
gnomAD v4: 5-135894973-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894973G>A , CM000667.2:g.135894973G>A GRCh38
NC_000005.9:g.135230662G>A , CM000667.1:g.135230662G>A GRCh37
NC_000005.8:g.135258561G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.183+467C>T MANE Select ENSP00000274520.1:n.183+467C>T
ENST00000274520.1:c.183+467C>T ENSP00000274520.1:n.183+467C>T
NM_000590.1:c.183+467C>T NP_000581.1:n.183+467C>T
NM_000590.2:c.183+467C>T MANE Select NP_000581.1:n.183+467C>T
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