Canonical Allele Identifier: CA388972097
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1470722880
gnomAD v2: 14-23844887-T-C
gnomAD v4: 14-23375678-T-C
MyVariant Identifiers: chr14:g.23844887T>C (hg19) chr14:g.23375678T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375678T>C , CM000676.2:g.23375678T>C GRCh38
NC_000014.8:g.23844887T>C , CM000676.1:g.23844887T>C GRCh37
NC_000014.7:g.22914727T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.284T>C MANE Select ENSP00000380417.2:p.Leu95Pro
ENST00000329715.2:c.332T>C ENSP00000328111.2:p.Leu111Pro
ENST00000397242.2:c.284T>C ENSP00000380417.2:p.Leu95Pro
NM_022789.3:c.332T>C NP_073626.1:p.Leu111Pro
NM_172314.1:c.284T>C NP_758525.1:p.Leu95Pro
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