ClinGen Allele Registry
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Canonical Allele Identifier:
CA405755630
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247595-T-A
MyVariant Identifiers:
chr19:g.39738235T>A (hg19)
chr19:g.39247595T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247595T>A , CM000681.2:g.39247595T>A
GRCh38
NC_000019.9:g.39738235T>A , CM000681.1:g.39738235T>A
GRCh37
NC_000019.8:g.44430075T>A
NCBI36
NG_042193.1:g.2377A>T
NG_055295.1:g.6262A>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.367+113A>T
ENSP00000476098.1:n.367+113A>T
ENST00000610963.1:c.366+113A>T
ENSP00000481371.1:n.366+113A>T
ENST00000616270.4:c.295A>T
ENSP00000480679.1:p.Ile99Phe
ENST00000634680.1:c.152-132A>T
ENSP00000489240.1:n.152-132A>T
ENST00000634967.1:c.224-132A>T
ENSP00000489559.1:n.224-132A>T
NR_074079.1:n.644+113A>T
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