Canonical Allele Identifier: CA485764097
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844888G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375679G>T , CM000676.2:g.23375679G>T GRCh38
NC_000014.8:g.23844888G>T , CM000676.1:g.23844888G>T GRCh37
NC_000014.7:g.22914728G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.285G>T MANE Select ENSP00000380417.2:p.Leu95=
ENST00000329715.2:c.333G>T ENSP00000328111.2:p.Leu111=
ENST00000397242.2:c.285G>T ENSP00000380417.2:p.Leu95=
NM_022789.3:c.333G>T NP_073626.1:p.Leu111=
NM_172314.1:c.285G>T NP_758525.1:p.Leu95=
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