Canonical Allele Identifier: CA405754970

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074954103
• gnomAD v4: 19-39247441-G-T
• MyVariant Identifiers: chr19:g.39738081G>T (hg19) ; chr19:g.39247441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247441G>T , CM000681.2:g.39247441G>T	GRCh38
NC_000019.9:g.39738081G>T , CM000681.1:g.39738081G>T	GRCh37
NC_000019.8:g.44429921G>T	NCBI36
NG_042193.1:g.2531C>A
NG_055295.1:g.6416C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.390C>A	ENSP00000476098.1:p.Leu130=
ENST00000610963.1:c.389C>A	ENSP00000481371.1:p.Ser130Tyr
ENST00000616270.4:c.422+27C>A	ENSP00000480679.1:n.422+27C>A
ENST00000634680.1:c.174C>A	ENSP00000489240.1:p.Leu58=
ENST00000634967.1:c.246C>A	ENSP00000489559.1:p.Leu82=
NR_074079.1:n.667C>A