Canonical Allele Identifier: CA405755015

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247453-G-T
• MyVariant Identifiers: chr19:g.39738093G>T (hg19) ; chr19:g.39247453G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247453G>T , CM000681.2:g.39247453G>T	GRCh38
NC_000019.9:g.39738093G>T , CM000681.1:g.39738093G>T	GRCh37
NC_000019.8:g.44429933G>T	NCBI36
NG_042193.1:g.2519C>A
NG_055295.1:g.6404C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.378C>A	ENSP00000476098.1:p.Gly126=
ENST00000610963.1:c.377C>A	ENSP00000481371.1:p.Ala126Glu
ENST00000616270.4:c.422+15C>A	ENSP00000480679.1:n.422+15C>A
ENST00000634680.1:c.162C>A	ENSP00000489240.1:p.Gly54=
ENST00000634967.1:c.234C>A	ENSP00000489559.1:p.Gly78=
NR_074079.1:n.655C>A