ClinGen Allele Registry
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Canonical Allele Identifier:
CA2814369731
Gene: IFNL4
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247470dup , CM000681.2:g.39247470dup
GRCh38
NC_000019.9:g.39738110dup , CM000681.1:g.39738110dup
GRCh37
NC_000019.8:g.44429950dup
NCBI36
NG_042193.1:g.2503dup
NG_055295.1:g.6388dup
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.368-6dup
ENSP00000476098.1:n.368-6dup
ENST00000610963.1:c.367-6dup
ENSP00000481371.1:n.367-6dup
ENST00000616270.4:c.421dup
ENSP00000480679.1:p.Leu141ProfsTer17
ENST00000634680.1:c.152-6dup
ENSP00000489240.1:n.152-6dup
ENST00000634967.1:c.224-6dup
ENSP00000489559.1:n.224-6dup
NR_074079.1:n.645-6dup
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