Canonical Allele Identifier: CA7113923
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1124053
ExAC: 14:23844979 C / A
gnomAD v2: 14-23844979-C-A
gnomAD v3: 14-23375770-C-A
gnomAD v4: 14-23375770-C-A
MyVariant Identifiers: chr14:g.23844979C>A (hg19) chr14:g.23375770C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375770C>A , CM000676.2:g.23375770C>A GRCh38
NC_000014.8:g.23844979C>A , CM000676.1:g.23844979C>A GRCh37
NC_000014.7:g.22914819C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000397242.3:c.376C>A MANE Select ENSP00000380417.2:p.Arg126=
ENST00000329715.2:c.424C>A ENSP00000328111.2:p.Arg142=
ENST00000397242.2:c.376C>A ENSP00000380417.2:p.Arg126=
NM_022789.3:c.424C>A NP_073626.1:p.Arg142=
NM_172314.1:c.376C>A NP_758525.1:p.Arg126=
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