Canonical Allele Identifier: CA7113877
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs781471351
ExAC: 14:23844789 T / C
gnomAD v2: 14-23844789-T-C
gnomAD v4: 14-23375580-T-C
MyVariant Identifiers: chr14:g.23844789T>C (hg19) chr14:g.23375580T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375580T>C , CM000676.2:g.23375580T>C GRCh38
NC_000014.8:g.23844789T>C , CM000676.1:g.23844789T>C GRCh37
NC_000014.7:g.22914629T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-45T>C MANE Select ENSP00000380417.2:n.231-45T>C
ENST00000329715.2:c.279-45T>C ENSP00000328111.2:n.279-45T>C
ENST00000397242.2:c.231-45T>C ENSP00000380417.2:n.231-45T>C
NM_022789.3:c.279-45T>C NP_073626.1:n.279-45T>C
NM_172314.1:c.231-45T>C NP_758525.1:n.231-45T>C
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