Canonical Allele Identifier: CA388972402
Gene: IL25 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.326A>G MANE Select ENSP00000380417.2:p.Asp109Gly
ENST00000329715.2:c.374A>G ENSP00000328111.2:p.Asp125Gly
ENST00000397242.2:c.326A>G ENSP00000380417.2:p.Asp109Gly
NM_022789.3:c.374A>G NP_073626.1:p.Asp125Gly
NM_172314.1:c.326A>G NP_758525.1:p.Asp109Gly
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