Canonical Allele Identifier: CA7982018
Community Standard Title: NM_145659.3(IL27):c.356T>C (p.Leu119Pro)
Gene: IL27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28502082A>G , CM000678.2:g.28502082A>G GRCh38
NC_000016.9:g.28513403A>G , CM000678.1:g.28513403A>G GRCh37
NC_000016.8:g.28420904A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_145659.3:c.356T>C MANE Select NP_663634.2:p.Leu119Pro
ENST00000356897.1:c.356T>C MANE Select ENSP00000349365.1:p.Leu119Pro
ENST00000568075.1:c.-38T>C ENSP00000455990.1:n.-38T>C
XM_011545780.1:c.362T>C XP_011544082.1:p.Leu121Pro
XM_011545780.2:c.362T>C XP_011544082.1:p.Leu121Pro
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