Canonical Allele Identifier: CA7113882
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs745828729
ExAC: 14:23844823 C / T
gnomAD v2: 14-23844823-C-T
gnomAD v3: 14-23375614-C-T
gnomAD v4: 14-23375614-C-T
COSMIC: COSN26442390
MyVariant Identifiers: chr14:g.23844823C>T (hg19) chr14:g.23375614C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375614C>T , CM000676.2:g.23375614C>T GRCh38
NC_000014.8:g.23844823C>T , CM000676.1:g.23844823C>T GRCh37
NC_000014.7:g.22914663C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-11C>T MANE Select ENSP00000380417.2:n.231-11C>T
ENST00000329715.2:c.279-11C>T ENSP00000328111.2:n.279-11C>T
ENST00000397242.2:c.231-11C>T ENSP00000380417.2:n.231-11C>T
NM_022789.3:c.279-11C>T NP_073626.1:n.279-11C>T
NM_172314.1:c.231-11C>T NP_758525.1:n.231-11C>T
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