Canonical Allele Identifier: CA2123434641
Gene: IL25 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375636A= , CM000676.2:g.23375636A= GRCh38
NC_000014.8:g.23844845A= , CM000676.1:g.23844845A= GRCh37
NC_000014.7:g.22914685A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.242A= MANE Select ENSP00000380417.2:p.Asp81=
ENST00000329715.2:c.290A= ENSP00000328111.2:p.Asp97=
ENST00000397242.2:c.242A= ENSP00000380417.2:p.Asp81=
NM_022789.3:c.290A= NP_073626.1:p.Asp97=
NM_172314.1:c.242A= NP_758525.1:p.Asp81=
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