Canonical Allele Identifier: CA485764118
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs758400379
MyVariant Identifiers: chr14:g.23844894G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375685G>T , CM000676.2:g.23375685G>T GRCh38
NC_000014.8:g.23844894G>T , CM000676.1:g.23844894G>T GRCh37
NC_000014.7:g.22914734G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.291G>T MANE Select ENSP00000380417.2:p.Pro97=
ENST00000329715.2:c.339G>T ENSP00000328111.2:p.Pro113=
ENST00000397242.2:c.291G>T ENSP00000380417.2:p.Pro97=
NM_022789.3:c.339G>T NP_073626.1:p.Pro113=
NM_172314.1:c.291G>T NP_758525.1:p.Pro97=
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