Canonical Allele Identifier: CA704269087
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1214026670
gnomAD v3: 14-23375582-T-G
gnomAD v4: 14-23375582-T-G
MyVariant Identifiers: chr14:g.23844791T>G (hg19) chr14:g.23375582T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375582T>G , CM000676.2:g.23375582T>G GRCh38
NC_000014.8:g.23844791T>G , CM000676.1:g.23844791T>G GRCh37
NC_000014.7:g.22914631T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-43T>G MANE Select ENSP00000380417.2:n.231-43T>G
ENST00000329715.2:c.279-43T>G ENSP00000328111.2:n.279-43T>G
ENST00000397242.2:c.231-43T>G ENSP00000380417.2:n.231-43T>G
NM_022789.3:c.279-43T>G NP_073626.1:n.279-43T>G
NM_172314.1:c.231-43T>G NP_758525.1:n.231-43T>G
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