Canonical Allele Identifier: CA388972396
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1595037453
gnomAD v4: 14-23375720-A-C
MyVariant Identifiers: chr14:g.23844929A>C (hg19) chr14:g.23375720A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375720A>C , CM000676.2:g.23375720A>C GRCh38
NC_000014.8:g.23844929A>C , CM000676.1:g.23844929A>C GRCh37
NC_000014.7:g.22914769A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.326A>C MANE Select ENSP00000380417.2:p.Asp109Ala
ENST00000329715.2:c.374A>C ENSP00000328111.2:p.Asp125Ala
ENST00000397242.2:c.326A>C ENSP00000380417.2:p.Asp109Ala
NM_022789.3:c.374A>C NP_073626.1:p.Asp125Ala
NM_172314.1:c.326A>C NP_758525.1:p.Asp109Ala
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