Canonical Allele Identifier: CA405754996

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247448-G-A
• MyVariant Identifiers: chr19:g.39738088G>A (hg19) ; chr19:g.39247448G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247448G>A , CM000681.2:g.39247448G>A	GRCh38
NC_000019.9:g.39738088G>A , CM000681.1:g.39738088G>A	GRCh37
NC_000019.8:g.44429928G>A	NCBI36
NG_042193.1:g.2524C>T
NG_055295.1:g.6409C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.383C>T	ENSP00000476098.1:p.Ala128Val
ENST00000610963.1:c.382C>T	ENSP00000481371.1:p.Pro128Ser
ENST00000616270.4:c.422+20C>T	ENSP00000480679.1:n.422+20C>T
ENST00000634680.1:c.167C>T	ENSP00000489240.1:p.Ala56Val
ENST00000634967.1:c.239C>T	ENSP00000489559.1:p.Ala80Val
NR_074079.1:n.660C>T