Canonical Allele Identifier: CA804328156
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1164036982
gnomAD v3: 5-135894877-T-G
gnomAD v4: 5-135894877-T-G
MyVariant Identifiers: chr5:g.135230566T>G (hg19) chr5:g.135894877T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894877T>G , CM000667.2:g.135894877T>G GRCh38
NC_000005.9:g.135230566T>G , CM000667.1:g.135230566T>G GRCh37
NC_000005.8:g.135258465T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.183+563A>C MANE Select ENSP00000274520.1:n.183+563A>C
ENST00000274520.1:c.183+563A>C ENSP00000274520.1:n.183+563A>C
NM_000590.1:c.183+563A>C NP_000581.1:n.183+563A>C
NM_000590.2:c.183+563A>C MANE Select NP_000581.1:n.183+563A>C
Search 100 bp 5'
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