Canonical Allele Identifier: CA405756285

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738427A>T (hg19) ; chr19:g.39247787A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247787A>T , CM000681.2:g.39247787A>T	GRCh38
NC_000019.9:g.39738427A>T , CM000681.1:g.39738427A>T	GRCh37
NC_000019.8:g.44430267A>T	NCBI36
NG_042193.1:g.2185T>A
NG_055295.1:g.6070T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.288T>A	ENSP00000476098.1:p.Pro96=
ENST00000610963.1:c.287T>A	ENSP00000481371.1:p.Leu96Gln
ENST00000616270.4:c.224-121T>A	ENSP00000480679.1:n.224-121T>A
ENST00000634680.1:c.152-324T>A	ENSP00000489240.1:n.152-324T>A
ENST00000634967.1:c.223+137T>A	ENSP00000489559.1:n.223+137T>A
NR_074079.1:n.565T>A