Canonical Allele Identifier: CA719670881
Gene: IL27 HGNC NCBI

Linked Data

dbSNP Id: rs1268803058

Genomic Alleles

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

Transcript Alleles

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