Canonical Allele Identifier: CA388972113
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375682-C-G
MyVariant Identifiers: chr14:g.23844891C>G (hg19) chr14:g.23375682C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375682C>G , CM000676.2:g.23375682C>G GRCh38
NC_000014.8:g.23844891C>G , CM000676.1:g.23844891C>G GRCh37
NC_000014.7:g.22914731C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.288C>G MANE Select ENSP00000380417.2:p.Cys96Trp
ENST00000329715.2:c.336C>G ENSP00000328111.2:p.Cys112Trp
ENST00000397242.2:c.288C>G ENSP00000380417.2:p.Cys96Trp
NM_022789.3:c.336C>G NP_073626.1:p.Cys112Trp
NM_172314.1:c.288C>G NP_758525.1:p.Cys96Trp
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