ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756875
Gene: IFNL4
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr19:g.39738620T>G (hg19)
chr19:g.39247980T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247980T>G , CM000681.2:g.39247980T>G
GRCh38
NC_000019.9:g.39738620T>G , CM000681.1:g.39738620T>G
GRCh37
NC_000019.8:g.44430460T>G
NCBI36
NG_042193.1:g.1992A>C
NG_055295.1:g.5877A>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.167A>C
ENSP00000476098.1:p.Glu56Ala
ENST00000610963.1:c.166A>C
ENSP00000481371.1:p.Ser56Arg
ENST00000616270.4:c.167A>C
ENSP00000480679.1:p.Glu56Ala
ENST00000634680.1:c.151+449A>C
ENSP00000489240.1:n.151+449A>C
ENST00000634967.1:c.167A>C
ENSP00000489559.1:p.Glu56Ala
NR_074079.1:n.444A>C
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