Canonical Allele Identifier: CA2123434933
Gene: IL25 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375870T= , CM000676.2:g.23375870T= GRCh38
NC_000014.8:g.23845079T= , CM000676.1:g.23845079T= GRCh37
NC_000014.7:g.22914919T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.476T= MANE Select ENSP00000380417.2:p.Val159=
ENST00000329715.2:c.524T= ENSP00000328111.2:p.Val175=
ENST00000397242.2:c.476T= ENSP00000380417.2:p.Val159=
NM_022789.3:c.524T= NP_073626.1:p.Val175=
NM_172314.1:c.476T= NP_758525.1:p.Val159=
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