Canonical Allele Identifier: CA388972614
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844960C>A (hg19) chr14:g.23375751C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375751C>A , CM000676.2:g.23375751C>A GRCh38
NC_000014.8:g.23844960C>A , CM000676.1:g.23844960C>A GRCh37
NC_000014.7:g.22914800C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.357C>A MANE Select ENSP00000380417.2:p.His119Gln
ENST00000329715.2:c.405C>A ENSP00000328111.2:p.His135Gln
ENST00000397242.2:c.357C>A ENSP00000380417.2:p.His119Gln
NM_022789.3:c.405C>A NP_073626.1:p.His135Gln
NM_172314.1:c.357C>A NP_758525.1:p.His119Gln
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