Canonical Allele Identifier: CA388972473
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844937G>T (hg19) chr14:g.23375728G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375728G>T , CM000676.2:g.23375728G>T GRCh38
NC_000014.8:g.23844937G>T , CM000676.1:g.23844937G>T GRCh37
NC_000014.7:g.22914777G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.334G>T MANE Select ENSP00000380417.2:p.Gly112Cys
ENST00000329715.2:c.382G>T ENSP00000328111.2:p.Gly128Cys
ENST00000397242.2:c.334G>T ENSP00000380417.2:p.Gly112Cys
NM_022789.3:c.382G>T NP_073626.1:p.Gly128Cys
NM_172314.1:c.334G>T NP_758525.1:p.Gly112Cys
Search 100 bp 5'
Search 100 bp 3'