Canonical Allele Identifier: CA2215668068
Gene: IL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506361G= , CM000678.2:g.28506361G= GRCh38
NC_000016.9:g.28517682G= , CM000678.1:g.28517682G= GRCh37
NC_000016.8:g.28425183G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+420C= MANE Select ENSP00000349365.1:n.31+420C=
ENST00000568075.1:c.-362-2311C= ENSP00000455990.1:n.-362-2311C=
NM_145659.3:c.31+420C= MANE Select NP_663634.2:n.31+420C=
XM_011545780.1:c.38-2311C= XP_011544082.1:n.38-2311C=
XM_011545780.2:c.38-2311C= XP_011544082.1:n.38-2311C=