Canonical Allele Identifier: CA388971930
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844869T>G (hg19) chr14:g.23375660T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375660T>G , CM000676.2:g.23375660T>G GRCh38
NC_000014.8:g.23844869T>G , CM000676.1:g.23844869T>G GRCh37
NC_000014.7:g.22914709T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.266T>G MANE Select ENSP00000380417.2:p.Leu89Arg
ENST00000329715.2:c.314T>G ENSP00000328111.2:p.Leu105Arg
ENST00000397242.2:c.266T>G ENSP00000380417.2:p.Leu89Arg
NM_022789.3:c.314T>G NP_073626.1:p.Leu105Arg
NM_172314.1:c.266T>G NP_758525.1:p.Leu89Arg
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