Canonical Allele Identifier: CA7113895
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs559504576
ExAC: 14:23844877 G / A
gnomAD v2: 14-23844877-G-A
gnomAD v3: 14-23375668-G-A
gnomAD v4: 14-23375668-G-A
MyVariant Identifiers: chr14:g.23844877G>A (hg19) chr14:g.23375668G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375668G>A , CM000676.2:g.23375668G>A GRCh38
NC_000014.8:g.23844877G>A , CM000676.1:g.23844877G>A GRCh37
NC_000014.7:g.22914717G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.274G>A MANE Select ENSP00000380417.2:p.Ala92Thr
ENST00000329715.2:c.322G>A ENSP00000328111.2:p.Ala108Thr
ENST00000397242.2:c.274G>A ENSP00000380417.2:p.Ala92Thr
NM_022789.3:c.322G>A NP_073626.1:p.Ala108Thr
NM_172314.1:c.274G>A NP_758525.1:p.Ala92Thr
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