Canonical Allele Identifier: CA279798554
Gene: IL27 HGNC NCBI

Linked Data

dbSNP Id: rs898368379
gnomAD v2: 16-28517613-C-G
gnomAD v3: 16-28506292-C-G
gnomAD v4: 16-28506292-C-G
MyVariant Identifiers: chr16:g.28517613C>G (hg19) chr16:g.28506292C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506292C>G , CM000678.2:g.28506292C>G GRCh38
NC_000016.9:g.28517613C>G , CM000678.1:g.28517613C>G GRCh37
NC_000016.8:g.28425114C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356897.1:c.31+489G>C MANE Select ENSP00000349365.1:n.31+489G>C
ENST00000568075.1:c.-362-2242G>C ENSP00000455990.1:n.-362-2242G>C
NM_145659.3:c.31+489G>C MANE Select NP_663634.2:n.31+489G>C
XM_011545780.1:c.38-2242G>C XP_011544082.1:n.38-2242G>C
XM_011545780.2:c.38-2242G>C XP_011544082.1:n.38-2242G>C
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