Canonical Allele Identifier: CA388971842
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1385220246
gnomAD v2: 14-23844859-C-T
gnomAD v4: 14-23375650-C-T
MyVariant Identifiers: chr14:g.23844859C>T (hg19) chr14:g.23375650C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375650C>T , CM000676.2:g.23375650C>T GRCh38
NC_000014.8:g.23844859C>T , CM000676.1:g.23844859C>T GRCh37
NC_000014.7:g.22914699C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.256C>T MANE Select ENSP00000380417.2:p.Pro86Ser
ENST00000329715.2:c.304C>T ENSP00000328111.2:p.Pro102Ser
ENST00000397242.2:c.256C>T ENSP00000380417.2:p.Pro86Ser
NM_022789.3:c.304C>T NP_073626.1:p.Pro102Ser
NM_172314.1:c.256C>T NP_758525.1:p.Pro86Ser
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