Canonical Allele Identifier: CA507655485

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247449-C-T
• MyVariant Identifiers: chr19:g.39738089C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247449C>T , CM000681.2:g.39247449C>T	GRCh38
NC_000019.9:g.39738089C>T , CM000681.1:g.39738089C>T	GRCh37
NC_000019.8:g.44429929C>T	NCBI36
NG_042193.1:g.2523G>A
NG_055295.1:g.6408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.382G>A	ENSP00000476098.1:p.Ala128Thr
ENST00000610963.1:c.381G>A	ENSP00000481371.1:p.Arg127=
ENST00000616270.4:c.422+19G>A	ENSP00000480679.1:n.422+19G>A
ENST00000634680.1:c.166G>A	ENSP00000489240.1:p.Ala56Thr
ENST00000634967.1:c.238G>A	ENSP00000489559.1:p.Ala80Thr
NR_074079.1:n.659G>A