Canonical Allele Identifier: CA2215668050
Gene: IL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506310C= , CM000678.2:g.28506310C= GRCh38
NC_000016.9:g.28517631C= , CM000678.1:g.28517631C= GRCh37
NC_000016.8:g.28425132C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+471G= MANE Select ENSP00000349365.1:n.31+471G=
ENST00000568075.1:c.-362-2260G= ENSP00000455990.1:n.-362-2260G=
NM_145659.3:c.31+471G= MANE Select NP_663634.2:n.31+471G=
XM_011545780.1:c.38-2260G= XP_011544082.1:n.38-2260G=
XM_011545780.2:c.38-2260G= XP_011544082.1:n.38-2260G=