Canonical Allele Identifier: CA388972726
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1890535145
MyVariant Identifiers: chr14:g.23844975C>G (hg19) chr14:g.23375766C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375766C>G , CM000676.2:g.23375766C>G GRCh38
NC_000014.8:g.23844975C>G , CM000676.1:g.23844975C>G GRCh37
NC_000014.7:g.22914815C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.372C>G MANE Select ENSP00000380417.2:p.Phe124Leu
ENST00000329715.2:c.420C>G ENSP00000328111.2:p.Phe140Leu
ENST00000397242.2:c.372C>G ENSP00000380417.2:p.Phe124Leu
NM_022789.3:c.420C>G NP_073626.1:p.Phe140Leu
NM_172314.1:c.372C>G NP_758525.1:p.Phe124Leu
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