Canonical Allele Identifier: CA405755039

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247459-T-C
• MyVariant Identifiers: chr19:g.39738099T>C (hg19) ; chr19:g.39247459T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247459T>C , CM000681.2:g.39247459T>C	GRCh38
NC_000019.9:g.39738099T>C , CM000681.1:g.39738099T>C	GRCh37
NC_000019.8:g.44429939T>C	NCBI36
NG_042193.1:g.2513A>G
NG_055295.1:g.6398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.372A>G	ENSP00000476098.1:p.Ter124Trp
ENST00000610963.1:c.371A>G	ENSP00000481371.1:p.Glu124Gly
ENST00000616270.4:c.422+9A>G	ENSP00000480679.1:n.422+9A>G
ENST00000634680.1:c.156A>G	ENSP00000489240.1:p.Ter52Trp
ENST00000634967.1:c.228A>G	ENSP00000489559.1:p.Ter76Trp
NR_074079.1:n.649A>G