Canonical Allele Identifier: CA7113890
Gene: IL25 HGNC NCBI

Linked Data

ClinVar Variation Id: 2241620
ClinVar RCV Id: RCV004103548
dbSNP Id: rs747685813
ExAC: 14:23844868 C / G
gnomAD v2: 14-23844868-C-G
gnomAD v3: 14-23375659-C-G
gnomAD v4: 14-23375659-C-G
MyVariant Identifiers: chr14:g.23844868C>G (hg19) chr14:g.23375659C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375659C>G , CM000676.2:g.23375659C>G GRCh38
NC_000014.8:g.23844868C>G , CM000676.1:g.23844868C>G GRCh37
NC_000014.7:g.22914708C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.265C>G MANE Select ENSP00000380417.2:p.Leu89Val
ENST00000329715.2:c.313C>G ENSP00000328111.2:p.Leu105Val
ENST00000397242.2:c.265C>G ENSP00000380417.2:p.Leu89Val
NM_022789.3:c.313C>G NP_073626.1:p.Leu105Val
NM_172314.1:c.265C>G NP_758525.1:p.Leu89Val
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