Canonical Allele Identifier: CA405756651

Gene: IFNL4

Linked Data

• dbSNP Id: rs117648444
• gnomAD v3: 19-39247938-G-T
• gnomAD v4: 19-39247938-G-T
• MyVariant Identifiers: chr19:g.39738578G>T (hg19) ; chr19:g.39247938G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247938G>T , CM000681.2:g.39247938G>T	GRCh38
NC_000019.9:g.39738578G>T , CM000681.1:g.39738578G>T	GRCh37
NC_000019.8:g.44430418G>T	NCBI36
NG_042193.1:g.2034C>A
NG_055295.1:g.5919C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.209C>A	ENSP00000476098.1:p.Ser70Tyr
ENST00000610963.1:c.208C>A	ENSP00000481371.1:p.Pro70Thr
ENST00000616270.4:c.209C>A	ENSP00000480679.1:p.Ser70Tyr
ENST00000634680.1:c.152-475C>A	ENSP00000489240.1:n.152-475C>A
ENST00000634967.1:c.209C>A	ENSP00000489559.1:p.Ser70Tyr
NR_074079.1:n.486C>A