Canonical Allele Identifier: CA405756023

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247720-A-T
• MyVariant Identifiers: chr19:g.39738360A>T (hg19) ; chr19:g.39247720A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247720A>T , CM000681.2:g.39247720A>T	GRCh38
NC_000019.9:g.39738360A>T , CM000681.1:g.39738360A>T	GRCh37
NC_000019.8:g.44430200A>T	NCBI36
NG_042193.1:g.2252T>A
NG_055295.1:g.6137T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.355T>A	ENSP00000476098.1:p.Cys119Ser
ENST00000610963.1:c.354T>A	ENSP00000481371.1:p.Asp118Glu
ENST00000616270.4:c.224-54T>A	ENSP00000480679.1:n.224-54T>A
ENST00000634680.1:c.152-257T>A	ENSP00000489240.1:n.152-257T>A
ENST00000634967.1:c.223+204T>A	ENSP00000489559.1:n.223+204T>A
NR_074079.1:n.632T>A