Canonical Allele Identifier: CA405755038

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074954195
• gnomAD v3: 19-39247459-T-A
• gnomAD v4: 19-39247459-T-A
• MyVariant Identifiers: chr19:g.39738099T>A (hg19) ; chr19:g.39247459T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.372A>T	ENSP00000476098.1:p.Ter124Cys
ENST00000610963.1:c.371A>T	ENSP00000481371.1:p.Glu124Val
ENST00000616270.4:c.422+9A>T	ENSP00000480679.1:n.422+9A>T
ENST00000634680.1:c.156A>T	ENSP00000489240.1:p.Ter52Cys
ENST00000634967.1:c.228A>T	ENSP00000489559.1:p.Ter76Cys
NR_074079.1:n.649A>T