Canonical Allele Identifier: CA388972168
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375693-T-C
MyVariant Identifiers: chr14:g.23844902T>C (hg19) chr14:g.23375693T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375693T>C , CM000676.2:g.23375693T>C GRCh38
NC_000014.8:g.23844902T>C , CM000676.1:g.23844902T>C GRCh37
NC_000014.7:g.22914742T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.299T>C MANE Select ENSP00000380417.2:p.Val100Ala
ENST00000329715.2:c.347T>C ENSP00000328111.2:p.Val116Ala
ENST00000397242.2:c.299T>C ENSP00000380417.2:p.Val100Ala
NM_022789.3:c.347T>C NP_073626.1:p.Val116Ala
NM_172314.1:c.299T>C NP_758525.1:p.Val100Ala
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