Canonical Allele Identifier: CA7113937
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs766181482
ExAC: 14:23845019 A / G
gnomAD v2: 14-23845019-A-G
gnomAD v4: 14-23375810-A-G
MyVariant Identifiers: chr14:g.23845019A>G (hg19) chr14:g.23375810A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375810A>G , CM000676.2:g.23375810A>G GRCh38
NC_000014.8:g.23845019A>G , CM000676.1:g.23845019A>G GRCh37
NC_000014.7:g.22914859A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.416A>G MANE Select ENSP00000380417.2:p.Tyr139Cys
ENST00000329715.2:c.464A>G ENSP00000328111.2:p.Tyr155Cys
ENST00000397242.2:c.416A>G ENSP00000380417.2:p.Tyr139Cys
NM_022789.3:c.464A>G NP_073626.1:p.Tyr155Cys
NM_172314.1:c.416A>G NP_758525.1:p.Tyr139Cys
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