Canonical Allele Identifier: CA7113908

Gene: IL25

Linked Data

• dbSNP Id: rs769307442
• ExAC: 14:23844920 C / G
• gnomAD v2: 14-23844920-C-G
• gnomAD v3: 14-23375711-C-G
• gnomAD v4: 14-23375711-C-G
• MyVariant Identifiers: chr14:g.23844920C>G (hg19) ; chr14:g.23375711C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23375711C>G , CM000676.2:g.23375711C>G	GRCh38
NC_000014.8:g.23844920C>G , CM000676.1:g.23844920C>G	GRCh37
NC_000014.7:g.22914760C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397242.3:c.317C>G MANE Select	ENSP00000380417.2:p.Ser106Cys
ENST00000329715.2:c.365C>G	ENSP00000328111.2:p.Ser122Cys
ENST00000397242.2:c.317C>G	ENSP00000380417.2:p.Ser106Cys
NM_022789.3:c.365C>G	NP_073626.1:p.Ser122Cys
NM_172314.1:c.317C>G	NP_758525.1:p.Ser106Cys