Canonical Allele Identifier: CA388971730
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844841A>G (hg19) chr14:g.23375632A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375632A>G , CM000676.2:g.23375632A>G GRCh38
NC_000014.8:g.23844841A>G , CM000676.1:g.23844841A>G GRCh37
NC_000014.7:g.22914681A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.238A>G MANE Select ENSP00000380417.2:p.Arg80Gly
ENST00000329715.2:c.286A>G ENSP00000328111.2:p.Arg96Gly
ENST00000397242.2:c.238A>G ENSP00000380417.2:p.Arg80Gly
NM_022789.3:c.286A>G NP_073626.1:p.Arg96Gly
NM_172314.1:c.238A>G NP_758525.1:p.Arg80Gly
Search 100 bp 5'
Search 100 bp 3'