Canonical Allele Identifier: CA7113904
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs144470149
ExAC: 14:23844901 G / A
gnomAD v2: 14-23844901-G-A
gnomAD v3: 14-23375692-G-A
gnomAD v4: 14-23375692-G-A
COSMIC: COSM1369194
MyVariant Identifiers: chr14:g.23844901G>A (hg19) chr14:g.23375692G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375692G>A , CM000676.2:g.23375692G>A GRCh38
NC_000014.8:g.23844901G>A , CM000676.1:g.23844901G>A GRCh37
NC_000014.7:g.22914741G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.298G>A MANE Select ENSP00000380417.2:p.Val100Ile
ENST00000329715.2:c.346G>A ENSP00000328111.2:p.Val116Ile
ENST00000397242.2:c.298G>A ENSP00000380417.2:p.Val100Ile
NM_022789.3:c.346G>A NP_073626.1:p.Val116Ile
NM_172314.1:c.298G>A NP_758525.1:p.Val100Ile
Search 100 bp 5'
Search 100 bp 3'