Canonical Allele Identifier: CA7113895

Gene: IL25

Linked Data

• dbSNP Id: rs559504576
• ExAC: 14:23844877 G / A
• gnomAD v2: 14-23844877-G-A
• gnomAD v3: 14-23375668-G-A
• gnomAD v4: 14-23375668-G-A
• MyVariant Identifiers: chr14:g.23844877G>A (hg19) ; chr14:g.23375668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23375668G>A , CM000676.2:g.23375668G>A	GRCh38
NC_000014.8:g.23844877G>A , CM000676.1:g.23844877G>A	GRCh37
NC_000014.7:g.22914717G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397242.3:c.274G>A MANE Select	ENSP00000380417.2:p.Ala92Thr
ENST00000329715.2:c.322G>A	ENSP00000328111.2:p.Ala108Thr
ENST00000397242.2:c.274G>A	ENSP00000380417.2:p.Ala92Thr
NM_022789.3:c.322G>A	NP_073626.1:p.Ala108Thr
NM_172314.1:c.274G>A	NP_758525.1:p.Ala92Thr