Canonical Allele Identifier: CA128070604
Gene: IL9 HGNC NCBI

Linked Data

dbSNP Id: rs375112095
MyVariant Identifiers: chr5:g.135230660G>T (hg19) chr5:g.135894971G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.135894971G>T , CM000667.2:g.135894971G>T GRCh38
NC_000005.9:g.135230660G>T , CM000667.1:g.135230660G>T GRCh37
NC_000005.8:g.135258559G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274520.2:c.183+469C>A MANE Select ENSP00000274520.1:n.183+469C>A
ENST00000274520.1:c.183+469C>A ENSP00000274520.1:n.183+469C>A
NM_000590.1:c.183+469C>A NP_000581.1:n.183+469C>A
NM_000590.2:c.183+469C>A MANE Select NP_000581.1:n.183+469C>A
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