Canonical Allele Identifier: CA2575485436
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375622-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375622C>T , CM000676.2:g.23375622C>T GRCh38
NC_000014.8:g.23844831C>T , CM000676.1:g.23844831C>T GRCh37
NC_000014.7:g.22914671C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-3C>T MANE Select ENSP00000380417.2:n.231-3C>T
ENST00000329715.2:c.279-3C>T ENSP00000328111.2:n.279-3C>T
ENST00000397242.2:c.231-3C>T ENSP00000380417.2:n.231-3C>T
NM_022789.3:c.279-3C>T NP_073626.1:n.279-3C>T
NM_172314.1:c.231-3C>T NP_758525.1:n.231-3C>T
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