Canonical Allele Identifier: CA405755566

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247580-C-A
• MyVariant Identifiers: chr19:g.39738220C>A (hg19) ; chr19:g.39247580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247580C>A , CM000681.2:g.39247580C>A	GRCh38
NC_000019.9:g.39738220C>A , CM000681.1:g.39738220C>A	GRCh37
NC_000019.8:g.44430060C>A	NCBI36
NG_042193.1:g.2392G>T
NG_055295.1:g.6277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-117G>T	ENSP00000476098.1:n.368-117G>T
ENST00000610963.1:c.367-117G>T	ENSP00000481371.1:n.367-117G>T
ENST00000616270.4:c.310G>T	ENSP00000480679.1:p.Gly104Trp
ENST00000634680.1:c.152-117G>T	ENSP00000489240.1:n.152-117G>T
ENST00000634967.1:c.224-117G>T	ENSP00000489559.1:n.224-117G>T
NR_074079.1:n.645-117G>T