Canonical Allele Identifier: CA405756654

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247939-A-T
• MyVariant Identifiers: chr19:g.39738579A>T (hg19) ; chr19:g.39247939A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247939A>T , CM000681.2:g.39247939A>T	GRCh38
NC_000019.9:g.39738579A>T , CM000681.1:g.39738579A>T	GRCh37
NC_000019.8:g.44430419A>T	NCBI36
NG_042193.1:g.2033T>A
NG_055295.1:g.5918T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.208T>A	ENSP00000476098.1:p.Ser70Thr
ENST00000610963.1:c.207T>A	ENSP00000481371.1:p.Asp69Glu
ENST00000616270.4:c.208T>A	ENSP00000480679.1:p.Ser70Thr
ENST00000634680.1:c.152-476T>A	ENSP00000489240.1:n.152-476T>A
ENST00000634967.1:c.208T>A	ENSP00000489559.1:p.Ser70Thr
NR_074079.1:n.485T>A