Canonical Allele Identifier: CA507407605

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738435G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247795G>T , CM000681.2:g.39247795G>T	GRCh38
NC_000019.9:g.39738435G>T , CM000681.1:g.39738435G>T	GRCh37
NC_000019.8:g.44430275G>T	NCBI36
NG_042193.1:g.2177C>A
NG_055295.1:g.6062C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.280C>A	ENSP00000476098.1:p.Gln94Lys
ENST00000610963.1:c.279C>A	ENSP00000481371.1:p.Leu93=
ENST00000616270.4:c.224-129C>A	ENSP00000480679.1:n.224-129C>A
ENST00000634680.1:c.152-332C>A	ENSP00000489240.1:n.152-332C>A
ENST00000634967.1:c.223+129C>A	ENSP00000489559.1:n.223+129C>A
NR_074079.1:n.557C>A