Canonical Allele Identifier: CA128070555
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs935102602
gnomAD v3: 5-135894762-C-A
gnomAD v4: 5-135894762-C-A
MyVariant Identifiers: chr5:g.135894762C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894762C>A , CM000667.2:g.135894762C>A GRCh38
NC_000005.9:g.135230451C>A , CM000667.1:g.135230451C>A GRCh37
NC_000005.8:g.135258350C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.184-611G>T MANE Select ENSP00000274520.1:n.184-611G>T
ENST00000274520.1:c.184-611G>T ENSP00000274520.1:n.184-611G>T
NM_000590.1:c.184-611G>T NP_000581.1:n.184-611G>T
NM_000590.2:c.184-611G>T MANE Select NP_000581.1:n.184-611G>T
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