Canonical Allele Identifier: CA7113892
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs773659715
ExAC: 14:23844870 G / C
gnomAD v2: 14-23844870-G-C
gnomAD v4: 14-23375661-G-C
MyVariant Identifiers: chr14:g.23844870G>C (hg19) chr14:g.23375661G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375661G>C , CM000676.2:g.23375661G>C GRCh38
NC_000014.8:g.23844870G>C , CM000676.1:g.23844870G>C GRCh37
NC_000014.7:g.22914710G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.267G>C MANE Select ENSP00000380417.2:p.Leu89=
ENST00000329715.2:c.315G>C ENSP00000328111.2:p.Leu105=
ENST00000397242.2:c.267G>C ENSP00000380417.2:p.Leu89=
NM_022789.3:c.315G>C NP_073626.1:p.Leu105=
NM_172314.1:c.267G>C NP_758525.1:p.Leu89=
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