Canonical Allele Identifier: CA2215668069
Gene: IL27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506362T= , CM000678.2:g.28506362T= GRCh38
NC_000016.9:g.28517683T= , CM000678.1:g.28517683T= GRCh37
NC_000016.8:g.28425184T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+419A= MANE Select ENSP00000349365.1:n.31+419A=
ENST00000568075.1:c.-362-2312A= ENSP00000455990.1:n.-362-2312A=
NM_145659.3:c.31+419A= MANE Select NP_663634.2:n.31+419A=
XM_011545780.1:c.38-2312A= XP_011544082.1:n.38-2312A=
XM_011545780.2:c.38-2312A= XP_011544082.1:n.38-2312A=
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