Canonical Allele Identifier: CA485764024
Gene: IL25 HGNC NCBI

Linked Data

COSMIC: COSM3495142
MyVariant Identifiers: chr14:g.23844835T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375626T>C , CM000676.2:g.23375626T>C GRCh38
NC_000014.8:g.23844835T>C , CM000676.1:g.23844835T>C GRCh37
NC_000014.7:g.22914675T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.232T>C MANE Select ENSP00000380417.2:p.Leu78=
ENST00000329715.2:c.280T>C ENSP00000328111.2:p.Leu94=
ENST00000397242.2:c.232T>C ENSP00000380417.2:p.Leu78=
NM_022789.3:c.280T>C NP_073626.1:p.Leu94=
NM_172314.1:c.232T>C NP_758525.1:p.Leu78=
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