Canonical Allele Identifier: CA7113906
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs147433946
ExAC: 14:23844912 G / A
gnomAD v2: 14-23844912-G-A
gnomAD v3: 14-23375703-G-A
gnomAD v4: 14-23375703-G-A
MyVariant Identifiers: chr14:g.23844912G>A (hg19) chr14:g.23375703G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375703G>A , CM000676.2:g.23375703G>A GRCh38
NC_000014.8:g.23844912G>A , CM000676.1:g.23844912G>A GRCh37
NC_000014.7:g.22914752G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.309G>A MANE Select ENSP00000380417.2:p.Gln103=
ENST00000329715.2:c.357G>A ENSP00000328111.2:p.Gln119=
ENST00000397242.2:c.309G>A ENSP00000380417.2:p.Gln103=
NM_022789.3:c.357G>A NP_073626.1:p.Gln119=
NM_172314.1:c.309G>A NP_758525.1:p.Gln103=
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