Canonical Allele Identifier: CA405755925

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247661-G-T
• MyVariant Identifiers: chr19:g.39738301G>T (hg19) ; chr19:g.39247661G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247661G>T , CM000681.2:g.39247661G>T	GRCh38
NC_000019.9:g.39738301G>T , CM000681.1:g.39738301G>T	GRCh37
NC_000019.8:g.44430141G>T	NCBI36
NG_042193.1:g.2311C>A
NG_055295.1:g.6196C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+47C>A	ENSP00000476098.1:n.367+47C>A
ENST00000610963.1:c.366+47C>A	ENSP00000481371.1:n.366+47C>A
ENST00000616270.4:c.229C>A	ENSP00000480679.1:p.Leu77Met
ENST00000634680.1:c.152-198C>A	ENSP00000489240.1:n.152-198C>A
ENST00000634967.1:c.224-198C>A	ENSP00000489559.1:n.224-198C>A
NR_074079.1:n.644+47C>A