Canonical Allele Identifier: CA2123434795
Gene: IL25 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375760T= , CM000676.2:g.23375760T= GRCh38
NC_000014.8:g.23844969T= , CM000676.1:g.23844969T= GRCh37
NC_000014.7:g.22914809T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.366T= MANE Select ENSP00000380417.2:p.Thr122=
ENST00000329715.2:c.414T= ENSP00000328111.2:p.Thr138=
ENST00000397242.2:c.366T= ENSP00000380417.2:p.Thr122=
NM_022789.3:c.414T= NP_073626.1:p.Thr138=
NM_172314.1:c.366T= NP_758525.1:p.Thr122=
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