Canonical Allele Identifier: CA2215668054
Gene: IL27 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506320T= , CM000678.2:g.28506320T= GRCh38
NC_000016.9:g.28517641T= , CM000678.1:g.28517641T= GRCh37
NC_000016.8:g.28425142T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+461A= MANE Select ENSP00000349365.1:n.31+461A=
ENST00000568075.1:c.-362-2270A= ENSP00000455990.1:n.-362-2270A=
NM_145659.3:c.31+461A= MANE Select NP_663634.2:n.31+461A=
XM_011545780.1:c.38-2270A= XP_011544082.1:n.38-2270A=
XM_011545780.2:c.38-2270A= XP_011544082.1:n.38-2270A=
Search 100 bp 5'
Search 100 bp 3'