Canonical Allele Identifier: CA7113894
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs766959581
ExAC: 14:23844876 C / T
gnomAD v2: 14-23844876-C-T
gnomAD v3: 14-23375667-C-T
gnomAD v4: 14-23375667-C-T
COSMIC: COSM1323553
MyVariant Identifiers: chr14:g.23844876C>T (hg19) chr14:g.23375667C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375667C>T , CM000676.2:g.23375667C>T GRCh38
NC_000014.8:g.23844876C>T , CM000676.1:g.23844876C>T GRCh37
NC_000014.7:g.22914716C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.273C>T MANE Select ENSP00000380417.2:p.His91=
ENST00000329715.2:c.321C>T ENSP00000328111.2:p.His107=
ENST00000397242.2:c.273C>T ENSP00000380417.2:p.His91=
NM_022789.3:c.321C>T NP_073626.1:p.His107=
NM_172314.1:c.273C>T NP_758525.1:p.His91=
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