Canonical Allele Identifier: CA2215668042
Gene: IL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506292C= , CM000678.2:g.28506292C= GRCh38
NC_000016.9:g.28517613C= , CM000678.1:g.28517613C= GRCh37
NC_000016.8:g.28425114C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356897.1:c.31+489G= MANE Select ENSP00000349365.1:n.31+489G=
ENST00000568075.1:c.-362-2242G= ENSP00000455990.1:n.-362-2242G=
NM_145659.3:c.31+489G= MANE Select NP_663634.2:n.31+489G=
XM_011545780.1:c.38-2242G= XP_011544082.1:n.38-2242G=
XM_011545780.2:c.38-2242G= XP_011544082.1:n.38-2242G=