Canonical Allele Identifier: CA405756483

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247835-C-T
• MyVariant Identifiers: chr19:g.39738475C>T (hg19) ; chr19:g.39247835C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247835C>T , CM000681.2:g.39247835C>T	GRCh38
NC_000019.9:g.39738475C>T , CM000681.1:g.39738475C>T	GRCh37
NC_000019.8:g.44430315C>T	NCBI36
NG_042193.1:g.2137G>A
NG_055295.1:g.6022G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.240G>A	ENSP00000476098.1:p.Pro80=
ENST00000610963.1:c.239G>A	ENSP00000481371.1:p.Arg80His
ENST00000616270.4:c.223+89G>A	ENSP00000480679.1:n.223+89G>A
ENST00000634680.1:c.152-372G>A	ENSP00000489240.1:n.152-372G>A
ENST00000634967.1:c.223+89G>A	ENSP00000489559.1:n.223+89G>A
NR_074079.1:n.517G>A