Canonical Allele Identifier: CA388972374
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375716-A-T
MyVariant Identifiers: chr14:g.23844925A>T (hg19) chr14:g.23375716A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375716A>T , CM000676.2:g.23375716A>T GRCh38
NC_000014.8:g.23844925A>T , CM000676.1:g.23844925A>T GRCh37
NC_000014.7:g.22914765A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.322A>T MANE Select ENSP00000380417.2:p.Met108Leu
ENST00000329715.2:c.370A>T ENSP00000328111.2:p.Met124Leu
ENST00000397242.2:c.322A>T ENSP00000380417.2:p.Met108Leu
NM_022789.3:c.370A>T NP_073626.1:p.Met124Leu
NM_172314.1:c.322A>T NP_758525.1:p.Met108Leu
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