Canonical Allele Identifier: CA388972538
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844943T>A (hg19) chr14:g.23375734T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375734T>A , CM000676.2:g.23375734T>A GRCh38
NC_000014.8:g.23844943T>A , CM000676.1:g.23844943T>A GRCh37
NC_000014.7:g.22914783T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.340T>A MANE Select ENSP00000380417.2:p.Ser114Thr
ENST00000329715.2:c.388T>A ENSP00000328111.2:p.Ser130Thr
ENST00000397242.2:c.340T>A ENSP00000380417.2:p.Ser114Thr
NM_022789.3:c.388T>A NP_073626.1:p.Ser130Thr
NM_172314.1:c.340T>A NP_758525.1:p.Ser114Thr
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