Canonical Allele Identifier: CA485763894
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844982C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375773C>A , CM000676.2:g.23375773C>A GRCh38
NC_000014.8:g.23844982C>A , CM000676.1:g.23844982C>A GRCh37
NC_000014.7:g.22914822C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.379C>A MANE Select ENSP00000380417.2:p.Arg127=
ENST00000329715.2:c.427C>A ENSP00000328111.2:p.Arg143=
ENST00000397242.2:c.379C>A ENSP00000380417.2:p.Arg127=
NM_022789.3:c.427C>A NP_073626.1:p.Arg143=
NM_172314.1:c.379C>A NP_758525.1:p.Arg127=
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