Canonical Allele Identifier: CA7113891
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs770223596
ExAC: 14:23844869 T / C
gnomAD v2: 14-23844869-T-C
gnomAD v3: 14-23375660-T-C
gnomAD v4: 14-23375660-T-C
MyVariant Identifiers: chr14:g.23844869T>C (hg19) chr14:g.23375660T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375660T>C , CM000676.2:g.23375660T>C GRCh38
NC_000014.8:g.23844869T>C , CM000676.1:g.23844869T>C GRCh37
NC_000014.7:g.22914709T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.266T>C MANE Select ENSP00000380417.2:p.Leu89Pro
ENST00000329715.2:c.314T>C ENSP00000328111.2:p.Leu105Pro
ENST00000397242.2:c.266T>C ENSP00000380417.2:p.Leu89Pro
NM_022789.3:c.314T>C NP_073626.1:p.Leu105Pro
NM_172314.1:c.266T>C NP_758525.1:p.Leu89Pro
Search 100 bp 5'
Search 100 bp 3'