Canonical Allele Identifier: CA485764239

Gene: IL25

Linked Data

• MyVariant Identifiers: chr14:g.23844939C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23375730C>G , CM000676.2:g.23375730C>G	GRCh38
NC_000014.8:g.23844939C>G , CM000676.1:g.23844939C>G	GRCh37
NC_000014.7:g.22914779C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397242.3:c.336C>G MANE Select	ENSP00000380417.2:p.Gly112=
ENST00000329715.2:c.384C>G	ENSP00000328111.2:p.Gly128=
ENST00000397242.2:c.336C>G	ENSP00000380417.2:p.Gly112=
NM_022789.3:c.384C>G	NP_073626.1:p.Gly128=
NM_172314.1:c.336C>G	NP_758525.1:p.Gly112=