Canonical Allele Identifier: CA405754990

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247447-G-A
• MyVariant Identifiers: chr19:g.39738087G>A (hg19) ; chr19:g.39247447G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247447G>A , CM000681.2:g.39247447G>A	GRCh38
NC_000019.9:g.39738087G>A , CM000681.1:g.39738087G>A	GRCh37
NC_000019.8:g.44429927G>A	NCBI36
NG_042193.1:g.2525C>T
NG_055295.1:g.6410C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.384C>T	ENSP00000476098.1:p.Ala128=
ENST00000610963.1:c.383C>T	ENSP00000481371.1:p.Pro128Leu
ENST00000616270.4:c.422+21C>T	ENSP00000480679.1:n.422+21C>T
ENST00000634680.1:c.168C>T	ENSP00000489240.1:p.Ala56=
ENST00000634967.1:c.240C>T	ENSP00000489559.1:p.Ala80=
NR_074079.1:n.661C>T