Canonical Allele Identifier: CA804328137
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs1217484586
MyVariant Identifiers: chr5:g.135230490T>C (hg19) chr5:g.135894801T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894801T>C , CM000667.2:g.135894801T>C GRCh38
NC_000005.9:g.135230490T>C , CM000667.1:g.135230490T>C GRCh37
NC_000005.8:g.135258389T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274520.2:c.183+639A>G MANE Select ENSP00000274520.1:n.183+639A>G
ENST00000274520.1:c.183+639A>G ENSP00000274520.1:n.183+639A>G
NM_000590.1:c.183+639A>G NP_000581.1:n.183+639A>G
NM_000590.2:c.183+639A>G MANE Select NP_000581.1:n.183+639A>G
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