Canonical Allele Identifier: CA485764293
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844954C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375745C>A , CM000676.2:g.23375745C>A GRCh38
NC_000014.8:g.23844954C>A , CM000676.1:g.23844954C>A GRCh37
NC_000014.7:g.22914794C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.351C>A MANE Select ENSP00000380417.2:p.Leu117=
ENST00000329715.2:c.399C>A ENSP00000328111.2:p.Leu133=
ENST00000397242.2:c.351C>A ENSP00000380417.2:p.Leu117=
NM_022789.3:c.399C>A NP_073626.1:p.Leu133=
NM_172314.1:c.351C>A NP_758525.1:p.Leu117=
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