Canonical Allele Identifier: CA388971753
Gene: IL25 HGNC NCBI

Linked Data

ClinVar Variation Id: 3109341
ClinVar RCV Id: RCV004405208
COSMIC: COSM954686
MyVariant Identifiers: chr14:g.23844844G>T (hg19) chr14:g.23375635G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375635G>T , CM000676.2:g.23375635G>T GRCh38
NC_000014.8:g.23844844G>T , CM000676.1:g.23844844G>T GRCh37
NC_000014.7:g.22914684G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.241G>T MANE Select ENSP00000380417.2:p.Asp81Tyr
ENST00000329715.2:c.289G>T ENSP00000328111.2:p.Asp97Tyr
ENST00000397242.2:c.241G>T ENSP00000380417.2:p.Asp81Tyr
NM_022789.3:c.289G>T NP_073626.1:p.Asp97Tyr
NM_172314.1:c.241G>T NP_758525.1:p.Asp81Tyr
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