Canonical Allele Identifier: CA485764269
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs2138561511
MyVariant Identifiers: chr14:g.23844948G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375739G>A , CM000676.2:g.23375739G>A GRCh38
NC_000014.8:g.23844948G>A , CM000676.1:g.23844948G>A GRCh37
NC_000014.7:g.22914788G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.345G>A MANE Select ENSP00000380417.2:p.Glu115=
ENST00000329715.2:c.393G>A ENSP00000328111.2:p.Glu131=
ENST00000397242.2:c.345G>A ENSP00000380417.2:p.Glu115=
NM_022789.3:c.393G>A NP_073626.1:p.Glu131=
NM_172314.1:c.345G>A NP_758525.1:p.Glu115=
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