Canonical Allele Identifier: CA2123434662
Gene: IL25 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375653C= , CM000676.2:g.23375653C= GRCh38
NC_000014.8:g.23844862C= , CM000676.1:g.23844862C= GRCh37
NC_000014.7:g.22914702C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.259C= MANE Select ENSP00000380417.2:p.Gln87=
ENST00000329715.2:c.307C= ENSP00000328111.2:p.Gln103=
ENST00000397242.2:c.259C= ENSP00000380417.2:p.Gln87=
NM_022789.3:c.307C= NP_073626.1:p.Gln103=
NM_172314.1:c.259C= NP_758525.1:p.Gln87=
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