ClinGen Allele Registry
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Canonical Allele Identifier:
CA9426140
Gene: IFNL4
HGNC
NCBI
Linked Data
dbSNP Id:
rs117648444
ExAC:
19:39738578 G / A
gnomAD v2:
19-39738578-G-A
gnomAD v3:
19-39247938-G-A
gnomAD v4:
19-39247938-G-A
MyVariant Identifiers:
chr19:g.39738578G>A (hg19)
chr19:g.39247938G>A (hg38)
Allelic Epigenome:
Alellic Epigenome (raw data)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247938G>A , CM000681.2:g.39247938G>A
GRCh38
NC_000019.9:g.39738578G>A , CM000681.1:g.39738578G>A
GRCh37
NC_000019.8:g.44430418G>A
NCBI36
NG_042193.1:g.2034C>T
NG_055295.1:g.5919C>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000606380.2:c.209C>T
ENSP00000476098.1:p.Ser70Phe
ENST00000610963.1:c.208C>T
ENSP00000481371.1:p.Pro70Ser
ENST00000616270.4:c.209C>T
ENSP00000480679.1:p.Ser70Phe
ENST00000634680.1:c.152-475C>T
ENSP00000489240.1:n.152-475C>T
ENST00000634967.1:c.209C>T
ENSP00000489559.1:p.Ser70Phe
NR_074079.1:n.486C>T
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