Canonical Allele Identifier: CA7113932
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs372547550
ExAC: 14:23845008 C / T
gnomAD v2: 14-23845008-C-T
gnomAD v3: 14-23375799-C-T
gnomAD v4: 14-23375799-C-T
MyVariant Identifiers: chr14:g.23845008C>T (hg19) chr14:g.23375799C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375799C>T , CM000676.2:g.23375799C>T GRCh38
NC_000014.8:g.23845008C>T , CM000676.1:g.23845008C>T GRCh37
NC_000014.7:g.22914848C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.405C>T MANE Select ENSP00000380417.2:p.Thr135=
ENST00000329715.2:c.453C>T ENSP00000328111.2:p.Thr151=
ENST00000397242.2:c.405C>T ENSP00000380417.2:p.Thr135=
NM_022789.3:c.453C>T NP_073626.1:p.Thr151=
NM_172314.1:c.405C>T NP_758525.1:p.Thr135=
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