ClinGen Allele Registry
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Canonical Allele Identifier:
CA2582150880
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v3:
19-39247630-CG-C
gnomAD v4:
19-39247630-CG-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247631del , CM000681.2:g.39247631del
GRCh38
NC_000019.9:g.39738271del , CM000681.1:g.39738271del
GRCh37
NC_000019.8:g.44430111del
NCBI36
NG_042193.1:g.2341del
NG_055295.1:g.6226del
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.367+77del
ENSP00000476098.1:n.367+77del
ENST00000610963.1:c.366+77del
ENSP00000481371.1:n.366+77del
ENST00000616270.4:c.259del
ENSP00000480679.1:p.Arg87AlafsTer8
ENST00000634680.1:c.152-168del
ENSP00000489240.1:n.152-168del
ENST00000634967.1:c.224-168del
ENSP00000489559.1:n.224-168del
NR_074079.1:n.644+77del
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