Canonical Allele Identifier: CA613317335
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1450945918
gnomAD v2: 14-23844816-C-A
gnomAD v4: 14-23375607-C-A
MyVariant Identifiers: chr14:g.23844816C>A (hg19) chr14:g.23375607C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375607C>A , CM000676.2:g.23375607C>A GRCh38
NC_000014.8:g.23844816C>A , CM000676.1:g.23844816C>A GRCh37
NC_000014.7:g.22914656C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-18C>A MANE Select ENSP00000380417.2:n.231-18C>A
ENST00000329715.2:c.279-18C>A ENSP00000328111.2:n.279-18C>A
ENST00000397242.2:c.231-18C>A ENSP00000380417.2:n.231-18C>A
NM_022789.3:c.279-18C>A NP_073626.1:n.279-18C>A
NM_172314.1:c.231-18C>A NP_758525.1:n.231-18C>A
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