Canonical Allele Identifier: CA257770166
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs945829062
gnomAD v3: 14-23375688-C-T
gnomAD v4: 14-23375688-C-T
MyVariant Identifiers: chr14:g.23844897C>T (hg19) chr14:g.23375688C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375688C>T , CM000676.2:g.23375688C>T GRCh38
NC_000014.8:g.23844897C>T , CM000676.1:g.23844897C>T GRCh37
NC_000014.7:g.22914737C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.294C>T MANE Select ENSP00000380417.2:p.His98=
ENST00000329715.2:c.342C>T ENSP00000328111.2:p.His114=
ENST00000397242.2:c.294C>T ENSP00000380417.2:p.His98=
NM_022789.3:c.342C>T NP_073626.1:p.His114=
NM_172314.1:c.294C>T NP_758525.1:p.His98=
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