Canonical Allele Identifier: CA388972177
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844904A>T (hg19) chr14:g.23375695A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375695A>T , CM000676.2:g.23375695A>T GRCh38
NC_000014.8:g.23844904A>T , CM000676.1:g.23844904A>T GRCh37
NC_000014.7:g.22914744A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.301A>T MANE Select ENSP00000380417.2:p.Ser101Cys
ENST00000329715.2:c.349A>T ENSP00000328111.2:p.Ser117Cys
ENST00000397242.2:c.301A>T ENSP00000380417.2:p.Ser101Cys
NM_022789.3:c.349A>T NP_073626.1:p.Ser117Cys
NM_172314.1:c.301A>T NP_758525.1:p.Ser101Cys
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