Canonical Allele Identifier: CA7113899

Gene: IL25

Linked Data

• dbSNP Id: rs756243453
• ExAC: 14:23844882 T / C
• gnomAD v2: 14-23844882-T-C
• gnomAD v3: 14-23375673-T-C
• gnomAD v4: 14-23375673-T-C
• MyVariant Identifiers: chr14:g.23844882T>C (hg19) ; chr14:g.23375673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23375673T>C , CM000676.2:g.23375673T>C	GRCh38
NC_000014.8:g.23844882T>C , CM000676.1:g.23844882T>C	GRCh37
NC_000014.7:g.22914722T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397242.3:c.279T>C MANE Select	ENSP00000380417.2:p.Arg93=
ENST00000329715.2:c.327T>C	ENSP00000328111.2:p.Arg109=
ENST00000397242.2:c.279T>C	ENSP00000380417.2:p.Arg93=
NM_022789.3:c.327T>C	NP_073626.1:p.Arg109=
NM_172314.1:c.279T>C	NP_758525.1:p.Arg93=