Canonical Allele Identifier: CA976103087
Gene: IL27 HGNC NCBI

Linked Data

dbSNP Id: rs2046460810
gnomAD v3: 16-28506344-T-C
gnomAD v4: 16-28506344-T-C
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Genomic Alleles

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

Transcript Alleles

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