Canonical Allele Identifier: CA2584994701

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247661-G-A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+47C>T	ENSP00000476098.1:n.367+47C>T
ENST00000610963.1:c.366+47C>T	ENSP00000481371.1:n.366+47C>T
ENST00000616270.4:c.229C>T	ENSP00000480679.1:p.Leu77=
ENST00000634680.1:c.152-198C>T	ENSP00000489240.1:n.152-198C>T
ENST00000634967.1:c.224-198C>T	ENSP00000489559.1:n.224-198C>T
NR_074079.1:n.644+47C>T