Canonical Allele Identifier: CA405756315

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247793-C-T
• MyVariant Identifiers: chr19:g.39738433C>T (hg19) ; chr19:g.39247793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247793C>T , CM000681.2:g.39247793C>T	GRCh38
NC_000019.9:g.39738433C>T , CM000681.1:g.39738433C>T	GRCh37
NC_000019.8:g.44430273C>T	NCBI36
NG_042193.1:g.2179G>A
NG_055295.1:g.6064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.282G>A	ENSP00000476098.1:p.Gln94=
ENST00000610963.1:c.281G>A	ENSP00000481371.1:p.Ser94Asn
ENST00000616270.4:c.224-127G>A	ENSP00000480679.1:n.224-127G>A
ENST00000634680.1:c.152-330G>A	ENSP00000489240.1:n.152-330G>A
ENST00000634967.1:c.223+131G>A	ENSP00000489559.1:n.223+131G>A
NR_074079.1:n.559G>A