Canonical Allele Identifier: CA388972888
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23845000A>T (hg19) chr14:g.23375791A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375791A>T , CM000676.2:g.23375791A>T GRCh38
NC_000014.8:g.23845000A>T , CM000676.1:g.23845000A>T GRCh37
NC_000014.7:g.22914840A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.397A>T MANE Select ENSP00000380417.2:p.Lys133Ter
ENST00000329715.2:c.445A>T ENSP00000328111.2:p.Lys149Ter
ENST00000397242.2:c.397A>T ENSP00000380417.2:p.Lys133Ter
NM_022789.3:c.445A>T NP_073626.1:p.Lys149Ter
NM_172314.1:c.397A>T NP_758525.1:p.Lys133Ter
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