Canonical Allele Identifier: CA2043819703
Gene: IL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68202881T= , CM000674.2:g.68202881T= GRCh38
NC_000012.11:g.68596661T= , CM000674.1:g.68596661T= GRCh37
NC_000012.10:g.66882928T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000229134.5:c.364-798A= MANE Select ENSP00000229134.4:n.364-798A=
ENST00000229134.4:c.364-798A= ENSP00000229134.4:n.364-798A=
NM_018402.1:c.364-798A= NP_060872.1:n.364-798A=
XM_011538568.1:c.364-798A= XP_011536870.1:n.364-798A=
XR_945055.1:n.264+4153T=
XR_002957418.1:n.280+4153T=
NM_018402.2:c.364-798A= MANE Select NP_060872.1:n.364-798A=