Canonical Allele Identifier: CA388971936
Gene: IL25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375662T>C , CM000676.2:g.23375662T>C GRCh38
NC_000014.8:g.23844871T>C , CM000676.1:g.23844871T>C GRCh37
NC_000014.7:g.22914711T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.268T>C MANE Select ENSP00000380417.2:p.Tyr90His
ENST00000329715.2:c.316T>C ENSP00000328111.2:p.Tyr106His
ENST00000397242.2:c.268T>C ENSP00000380417.2:p.Tyr90His
NM_022789.3:c.316T>C NP_073626.1:p.Tyr106His
NM_172314.1:c.268T>C NP_758525.1:p.Tyr90His