Canonical Allele Identifier: CA405754962

Gene: IFNL4

Linked Data

• dbSNP Id: rs1407776204
• gnomAD v4: 19-39247438-G-T
• MyVariant Identifiers: chr19:g.39738078G>T (hg19) ; chr19:g.39247438G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247438G>T , CM000681.2:g.39247438G>T	GRCh38
NC_000019.9:g.39738078G>T , CM000681.1:g.39738078G>T	GRCh37
NC_000019.8:g.44429918G>T	NCBI36
NG_042193.1:g.2534C>A
NG_055295.1:g.6419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.393C>A	ENSP00000476098.1:p.Leu131=
ENST00000610963.1:c.392C>A	ENSP00000481371.1:p.Ser131Tyr
ENST00000616270.4:c.422+30C>A	ENSP00000480679.1:n.422+30C>A
ENST00000634680.1:c.177C>A	ENSP00000489240.1:p.Leu59=
ENST00000634967.1:c.249C>A	ENSP00000489559.1:p.Leu83=
NR_074079.1:n.670C>A