Canonical Allele Identifier: CA388972674
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844967A>T (hg19) chr14:g.23375758A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375758A>T , CM000676.2:g.23375758A>T GRCh38
NC_000014.8:g.23844967A>T , CM000676.1:g.23844967A>T GRCh37
NC_000014.7:g.22914807A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.364A>T MANE Select ENSP00000380417.2:p.Thr122Ser
ENST00000329715.2:c.412A>T ENSP00000328111.2:p.Thr138Ser
ENST00000397242.2:c.364A>T ENSP00000380417.2:p.Thr122Ser
NM_022789.3:c.412A>T NP_073626.1:p.Thr138Ser
NM_172314.1:c.364A>T NP_758525.1:p.Thr122Ser
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