Canonical Allele Identifier: CA388971734
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1890527059
gnomAD v3: 14-23375633-G-A
gnomAD v4: 14-23375633-G-A
MyVariant Identifiers: chr14:g.23844842G>A (hg19) chr14:g.23375633G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375633G>A , CM000676.2:g.23375633G>A GRCh38
NC_000014.8:g.23844842G>A , CM000676.1:g.23844842G>A GRCh37
NC_000014.7:g.22914682G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.239G>A MANE Select ENSP00000380417.2:p.Arg80Lys
ENST00000329715.2:c.287G>A ENSP00000328111.2:p.Arg96Lys
ENST00000397242.2:c.239G>A ENSP00000380417.2:p.Arg80Lys
NM_022789.3:c.287G>A NP_073626.1:p.Arg96Lys
NM_172314.1:c.239G>A NP_758525.1:p.Arg80Lys
Search 100 bp 5'
Search 100 bp 3'