Canonical Allele Identifier: CA7113903
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs779957438
ExAC: 14:23844896 A / G
gnomAD v2: 14-23844896-A-G
gnomAD v4: 14-23375687-A-G
MyVariant Identifiers: chr14:g.23844896A>G (hg19) chr14:g.23375687A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375687A>G , CM000676.2:g.23375687A>G GRCh38
NC_000014.8:g.23844896A>G , CM000676.1:g.23844896A>G GRCh37
NC_000014.7:g.22914736A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.293A>G MANE Select ENSP00000380417.2:p.His98Arg
ENST00000329715.2:c.341A>G ENSP00000328111.2:p.His114Arg
ENST00000397242.2:c.293A>G ENSP00000380417.2:p.His98Arg
NM_022789.3:c.341A>G NP_073626.1:p.His114Arg
NM_172314.1:c.293A>G NP_758525.1:p.His98Arg
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