Canonical Allele Identifier: CA485764222
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375724-C-T
MyVariant Identifiers: chr14:g.23844933C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375724C>T , CM000676.2:g.23375724C>T GRCh38
NC_000014.8:g.23844933C>T , CM000676.1:g.23844933C>T GRCh37
NC_000014.7:g.22914773C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.330C>T MANE Select ENSP00000380417.2:p.Pro110=
ENST00000329715.2:c.378C>T ENSP00000328111.2:p.Pro126=
ENST00000397242.2:c.330C>T ENSP00000380417.2:p.Pro110=
NM_022789.3:c.378C>T NP_073626.1:p.Pro126=
NM_172314.1:c.330C>T NP_758525.1:p.Pro110=
Search 100 bp 5'
Search 100 bp 3'