Canonical Allele Identifier: CA2584994684
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247590-CTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247591_39247592del , CM000681.2:g.39247591_39247592del GRCh38
NC_000019.9:g.39738231_39738232del , CM000681.1:g.39738231_39738232del GRCh37
NC_000019.8:g.44430071_44430072del NCBI36
NG_042193.1:g.2380_2381del
NG_055295.1:g.6265_6266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+116_367+117del ENSP00000476098.1:n.367+116_367+117del
ENST00000610963.1:c.366+116_366+117del ENSP00000481371.1:n.366+116_366+117del
ENST00000616270.4:c.298_299del ENSP00000480679.1:p.Gln100AspfsTer10
ENST00000634680.1:c.152-129_152-128del ENSP00000489240.1:n.152-129_152-128del
ENST00000634967.1:c.224-129_224-128del ENSP00000489559.1:n.224-129_224-128del
NR_074079.1:n.644+116_644+117del
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