Canonical Allele Identifier: CA388971959
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844874C>A (hg19) chr14:g.23375665C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375665C>A , CM000676.2:g.23375665C>A GRCh38
NC_000014.8:g.23844874C>A , CM000676.1:g.23844874C>A GRCh37
NC_000014.7:g.22914714C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.271C>A MANE Select ENSP00000380417.2:p.His91Asn
ENST00000329715.2:c.319C>A ENSP00000328111.2:p.His107Asn
ENST00000397242.2:c.271C>A ENSP00000380417.2:p.His91Asn
NM_022789.3:c.319C>A NP_073626.1:p.His107Asn
NM_172314.1:c.271C>A NP_758525.1:p.His91Asn
Search 100 bp 5'
Search 100 bp 3'