Canonical Allele Identifier: CA7113915
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs775411567
ExAC: 14:23844944 C / T
gnomAD v2: 14-23844944-C-T
gnomAD v3: 14-23375735-C-T
gnomAD v4: 14-23375735-C-T
COSMIC: COSM161719
MyVariant Identifiers: chr14:g.23844944C>T (hg19) chr14:g.23375735C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375735C>T , CM000676.2:g.23375735C>T GRCh38
NC_000014.8:g.23844944C>T , CM000676.1:g.23844944C>T GRCh37
NC_000014.7:g.22914784C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.341C>T MANE Select ENSP00000380417.2:p.Ser114Leu
ENST00000329715.2:c.389C>T ENSP00000328111.2:p.Ser130Leu
ENST00000397242.2:c.341C>T ENSP00000380417.2:p.Ser114Leu
NM_022789.3:c.389C>T NP_073626.1:p.Ser130Leu
NM_172314.1:c.341C>T NP_758525.1:p.Ser114Leu
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