Canonical Allele Identifier: CA388971699
Gene: IL25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375628G>T , CM000676.2:g.23375628G>T GRCh38
NC_000014.8:g.23844837G>T , CM000676.1:g.23844837G>T GRCh37
NC_000014.7:g.22914677G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.234G>T MANE Select ENSP00000380417.2:p.Leu78Phe
ENST00000329715.2:c.282G>T ENSP00000328111.2:p.Leu94Phe
ENST00000397242.2:c.234G>T ENSP00000380417.2:p.Leu78Phe
NM_022789.3:c.282G>T NP_073626.1:p.Leu94Phe
NM_172314.1:c.234G>T NP_758525.1:p.Leu78Phe