Canonical Allele Identifier: CA388972602
Gene: IL25 HGNC NCBI

Linked Data

gnomAD v4: 14-23375749-C-G
MyVariant Identifiers: chr14:g.23844958C>G (hg19) chr14:g.23375749C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375749C>G , CM000676.2:g.23375749C>G GRCh38
NC_000014.8:g.23844958C>G , CM000676.1:g.23844958C>G GRCh37
NC_000014.7:g.22914798C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.355C>G MANE Select ENSP00000380417.2:p.His119Asp
ENST00000329715.2:c.403C>G ENSP00000328111.2:p.His135Asp
ENST00000397242.2:c.355C>G ENSP00000380417.2:p.His119Asp
NM_022789.3:c.403C>G NP_073626.1:p.His135Asp
NM_172314.1:c.355C>G NP_758525.1:p.His119Asp
Search 100 bp 5'
Search 100 bp 3'