Canonical Allele Identifier: CA388972105
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844890G>A (hg19) chr14:g.23375681G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375681G>A , CM000676.2:g.23375681G>A GRCh38
NC_000014.8:g.23844890G>A , CM000676.1:g.23844890G>A GRCh37
NC_000014.7:g.22914730G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.287G>A MANE Select ENSP00000380417.2:p.Cys96Tyr
ENST00000329715.2:c.335G>A ENSP00000328111.2:p.Cys112Tyr
ENST00000397242.2:c.287G>A ENSP00000380417.2:p.Cys96Tyr
NM_022789.3:c.335G>A NP_073626.1:p.Cys112Tyr
NM_172314.1:c.287G>A NP_758525.1:p.Cys96Tyr
Search 100 bp 5'
Search 100 bp 3'