Canonical Allele Identifier: CA7113880
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs760489052
ExAC: 14:23844813 TGAC / T
gnomAD v2: 14-23844813-TGAC-T
gnomAD v4: 14-23375604-TGAC-T
MyVariant Identifiers: chr14:g.23844814_23844816del (hg19) chr14:g.23375605_23375607del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375605_23375607del , CM000676.2:g.23375605_23375607del GRCh38
NC_000014.8:g.23844814_23844816del , CM000676.1:g.23844814_23844816del GRCh37
NC_000014.7:g.22914654_22914656del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-20_231-18del MANE Select ENSP00000380417.2:n.231-20_231-18del
ENST00000329715.2:c.279-20_279-18del ENSP00000328111.2:n.279-20_279-18del
ENST00000397242.2:c.231-20_231-18del ENSP00000380417.2:n.231-20_231-18del
NM_022789.3:c.279-20_279-18del NP_073626.1:n.279-20_279-18del
NM_172314.1:c.231-20_231-18del NP_758525.1:n.231-20_231-18del
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