Canonical Allele Identifier: CA388972590
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844956A>C (hg19) chr14:g.23375747A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375747A>C , CM000676.2:g.23375747A>C GRCh38
NC_000014.8:g.23844956A>C , CM000676.1:g.23844956A>C GRCh37
NC_000014.7:g.22914796A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.353A>C MANE Select ENSP00000380417.2:p.Tyr118Ser
ENST00000329715.2:c.401A>C ENSP00000328111.2:p.Tyr134Ser
ENST00000397242.2:c.353A>C ENSP00000380417.2:p.Tyr118Ser
NM_022789.3:c.401A>C NP_073626.1:p.Tyr134Ser
NM_172314.1:c.353A>C NP_758525.1:p.Tyr118Ser
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