Canonical Allele Identifier: CA704269089
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1446130078
gnomAD v4: 14-23375598-A-G
MyVariant Identifiers: chr14:g.23844807A>G (hg19) chr14:g.23375598A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375598A>G , CM000676.2:g.23375598A>G GRCh38
NC_000014.8:g.23844807A>G , CM000676.1:g.23844807A>G GRCh37
NC_000014.7:g.22914647A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-27A>G MANE Select ENSP00000380417.2:n.231-27A>G
ENST00000329715.2:c.279-27A>G ENSP00000328111.2:n.279-27A>G
ENST00000397242.2:c.231-27A>G ENSP00000380417.2:n.231-27A>G
NM_022789.3:c.279-27A>G NP_073626.1:n.279-27A>G
NM_172314.1:c.231-27A>G NP_758525.1:n.231-27A>G
Search 100 bp 5'
Search 100 bp 3'