Canonical Allele Identifier: CA2123434654
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1890528113
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375653dup , CM000676.2:g.23375653dup GRCh38
NC_000014.8:g.23844862dup , CM000676.1:g.23844862dup GRCh37
NC_000014.7:g.22914702dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.259dup MANE Select ENSP00000380417.2:p.Gln87ProfsTer?
ENST00000329715.2:c.307dup ENSP00000328111.2:p.Gln103ProfsTer?
ENST00000397242.2:c.259dup ENSP00000380417.2:p.Gln87ProfsTer?
NM_022789.3:c.307dup NP_073626.1:p.Gln103ProfsTer?
NM_172314.1:c.259dup NP_758525.1:p.Gln87ProfsTer?
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