Canonical Allele Identifier: CA507655471

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738080G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247440G>T , CM000681.2:g.39247440G>T	GRCh38
NC_000019.9:g.39738080G>T , CM000681.1:g.39738080G>T	GRCh37
NC_000019.8:g.44429920G>T	NCBI36
NG_042193.1:g.2532C>A
NG_055295.1:g.6417C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.391C>A	ENSP00000476098.1:p.Leu131Ile
ENST00000610963.1:c.390C>A	ENSP00000481371.1:p.Ser130=
ENST00000616270.4:c.422+28C>A	ENSP00000480679.1:n.422+28C>A
ENST00000634680.1:c.175C>A	ENSP00000489240.1:p.Leu59Ile
ENST00000634967.1:c.247C>A	ENSP00000489559.1:p.Leu83Ile
NR_074079.1:n.668C>A