Canonical Allele Identifier: CA388971835
Gene: IL25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375648T>A , CM000676.2:g.23375648T>A GRCh38
NC_000014.8:g.23844857T>A , CM000676.1:g.23844857T>A GRCh37
NC_000014.7:g.22914697T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.254T>A MANE Select ENSP00000380417.2:p.Leu85His
ENST00000329715.2:c.302T>A ENSP00000328111.2:p.Leu101His
ENST00000397242.2:c.254T>A ENSP00000380417.2:p.Leu85His
NM_022789.3:c.302T>A NP_073626.1:p.Leu101His
NM_172314.1:c.254T>A NP_758525.1:p.Leu85His