Canonical Allele Identifier: CA388972672
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844967A>G (hg19) chr14:g.23375758A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375758A>G , CM000676.2:g.23375758A>G GRCh38
NC_000014.8:g.23844967A>G , CM000676.1:g.23844967A>G GRCh37
NC_000014.7:g.22914807A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.364A>G MANE Select ENSP00000380417.2:p.Thr122Ala
ENST00000329715.2:c.412A>G ENSP00000328111.2:p.Thr138Ala
ENST00000397242.2:c.364A>G ENSP00000380417.2:p.Thr122Ala
NM_022789.3:c.412A>G NP_073626.1:p.Thr138Ala
NM_172314.1:c.364A>G NP_758525.1:p.Thr122Ala
Search 100 bp 5'
Search 100 bp 3'