Canonical Allele Identifier: CA405755692

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738248T>A (hg19) ; chr19:g.39247608T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247608T>A , CM000681.2:g.39247608T>A	GRCh38
NC_000019.9:g.39738248T>A , CM000681.1:g.39738248T>A	GRCh37
NC_000019.8:g.44430088T>A	NCBI36
NG_042193.1:g.2364A>T
NG_055295.1:g.6249A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+100A>T	ENSP00000476098.1:n.367+100A>T
ENST00000610963.1:c.366+100A>T	ENSP00000481371.1:n.366+100A>T
ENST00000616270.4:c.282A>T	ENSP00000480679.1:p.Leu94Phe
ENST00000634680.1:c.152-145A>T	ENSP00000489240.1:n.152-145A>T
ENST00000634967.1:c.224-145A>T	ENSP00000489559.1:n.224-145A>T
NR_074079.1:n.644+100A>T