ClinGen Allele Registry
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Canonical Allele Identifier:
CA405755547
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247574-A-G
MyVariant Identifiers:
chr19:g.39738214A>G (hg19)
chr19:g.39247574A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247574A>G , CM000681.2:g.39247574A>G
GRCh38
NC_000019.9:g.39738214A>G , CM000681.1:g.39738214A>G
GRCh37
NC_000019.8:g.44430054A>G
NCBI36
NG_042193.1:g.2398T>C
NG_055295.1:g.6283T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.368-111T>C
ENSP00000476098.1:n.368-111T>C
ENST00000610963.1:c.367-111T>C
ENSP00000481371.1:n.367-111T>C
ENST00000616270.4:c.316T>C
ENSP00000480679.1:p.Ser106Pro
ENST00000634680.1:c.152-111T>C
ENSP00000489240.1:n.152-111T>C
ENST00000634967.1:c.224-111T>C
ENSP00000489559.1:n.224-111T>C
NR_074079.1:n.645-111T>C
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