Canonical Allele Identifier: CA7113888
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs145160878
ExAC: 14:23844853 C / A
gnomAD v2: 14-23844853-C-A
gnomAD v4: 14-23375644-C-A
MyVariant Identifiers: chr14:g.23844853C>A (hg19) chr14:g.23375644C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375644C>A , CM000676.2:g.23375644C>A GRCh38
NC_000014.8:g.23844853C>A , CM000676.1:g.23844853C>A GRCh37
NC_000014.7:g.22914693C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.250C>A MANE Select ENSP00000380417.2:p.Arg84=
ENST00000329715.2:c.298C>A ENSP00000328111.2:p.Arg100=
ENST00000397242.2:c.250C>A ENSP00000380417.2:p.Arg84=
NM_022789.3:c.298C>A NP_073626.1:p.Arg100=
NM_172314.1:c.250C>A NP_758525.1:p.Arg84=
Search 100 bp 5'
Search 100 bp 3'