Canonical Allele Identifier: CA7113889
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs776356526

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375647C>T , CM000676.2:g.23375647C>T GRCh38
NC_000014.8:g.23844856C>T , CM000676.1:g.23844856C>T GRCh37
NC_000014.7:g.22914696C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.253C>T MANE Select ENSP00000380417.2:p.Leu85Phe
ENST00000329715.2:c.301C>T ENSP00000328111.2:p.Leu101Phe
ENST00000397242.2:c.253C>T ENSP00000380417.2:p.Leu85Phe
NM_022789.3:c.301C>T NP_073626.1:p.Leu101Phe
NM_172314.1:c.253C>T NP_758525.1:p.Leu85Phe