Canonical Allele Identifier: CA388972718
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844974T>C (hg19) chr14:g.23375765T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375765T>C , CM000676.2:g.23375765T>C GRCh38
NC_000014.8:g.23844974T>C , CM000676.1:g.23844974T>C GRCh37
NC_000014.7:g.22914814T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.371T>C MANE Select ENSP00000380417.2:p.Phe124Ser
ENST00000329715.2:c.419T>C ENSP00000328111.2:p.Phe140Ser
ENST00000397242.2:c.371T>C ENSP00000380417.2:p.Phe124Ser
NM_022789.3:c.419T>C NP_073626.1:p.Phe140Ser
NM_172314.1:c.371T>C NP_758525.1:p.Phe124Ser
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