Canonical Allele Identifier: CA388972014
Gene: IL25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375667C>G , CM000676.2:g.23375667C>G GRCh38
NC_000014.8:g.23844876C>G , CM000676.1:g.23844876C>G GRCh37
NC_000014.7:g.22914716C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.273C>G MANE Select ENSP00000380417.2:p.His91Gln
ENST00000329715.2:c.321C>G ENSP00000328111.2:p.His107Gln
ENST00000397242.2:c.273C>G ENSP00000380417.2:p.His91Gln
NM_022789.3:c.321C>G NP_073626.1:p.His107Gln
NM_172314.1:c.273C>G NP_758525.1:p.His91Gln