Canonical Allele Identifier: CA279798561
Gene: IL27 HGNC NCBI

Linked Data

dbSNP Id: rs887030390
gnomAD v2: 16-28517641-T-A
gnomAD v3: 16-28506320-T-A
gnomAD v4: 16-28506320-T-A
MyVariant Identifiers: chr16:g.28517641T>A (hg19) chr16:g.28506320T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+461A>T MANE Select ENSP00000349365.1:n.31+461A>T
ENST00000568075.1:c.-362-2270A>T ENSP00000455990.1:n.-362-2270A>T
NM_145659.3:c.31+461A>T MANE Select NP_663634.2:n.31+461A>T
XM_011545780.1:c.38-2270A>T XP_011544082.1:n.38-2270A>T
XM_011545780.2:c.38-2270A>T XP_011544082.1:n.38-2270A>T
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