Canonical Allele Identifier: CA2215668062
Gene: IL27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506344T= , CM000678.2:g.28506344T= GRCh38
NC_000016.9:g.28517665T= , CM000678.1:g.28517665T= GRCh37
NC_000016.8:g.28425166T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+437A= MANE Select ENSP00000349365.1:n.31+437A=
ENST00000568075.1:c.-362-2294A= ENSP00000455990.1:n.-362-2294A=
NM_145659.3:c.31+437A= MANE Select NP_663634.2:n.31+437A=
XM_011545780.1:c.38-2294A= XP_011544082.1:n.38-2294A=
XM_011545780.2:c.38-2294A= XP_011544082.1:n.38-2294A=
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