Canonical Allele Identifier: CA405755192

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738131A>T (hg19) ; chr19:g.39247491A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247491A>T , CM000681.2:g.39247491A>T	GRCh38
NC_000019.9:g.39738131A>T , CM000681.1:g.39738131A>T	GRCh37
NC_000019.8:g.44429971A>T	NCBI36
NG_042193.1:g.2481T>A
NG_055295.1:g.6366T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-28T>A	ENSP00000476098.1:n.368-28T>A
ENST00000610963.1:c.367-28T>A	ENSP00000481371.1:n.367-28T>A
ENST00000616270.4:c.399T>A	ENSP00000480679.1:p.Phe133Leu
ENST00000634680.1:c.152-28T>A	ENSP00000489240.1:n.152-28T>A
ENST00000634967.1:c.224-28T>A	ENSP00000489559.1:n.224-28T>A
NR_074079.1:n.645-28T>A