Canonical Allele Identifier: CA388972172
Gene: IL25 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23844904A>C (hg19) chr14:g.23375695A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375695A>C , CM000676.2:g.23375695A>C GRCh38
NC_000014.8:g.23844904A>C , CM000676.1:g.23844904A>C GRCh37
NC_000014.7:g.22914744A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.301A>C MANE Select ENSP00000380417.2:p.Ser101Arg
ENST00000329715.2:c.349A>C ENSP00000328111.2:p.Ser117Arg
ENST00000397242.2:c.301A>C ENSP00000380417.2:p.Ser101Arg
NM_022789.3:c.349A>C NP_073626.1:p.Ser117Arg
NM_172314.1:c.301A>C NP_758525.1:p.Ser101Arg
Search 100 bp 5'
Search 100 bp 3'