Canonical Allele Identifier: CA405755041

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738099T>G (hg19) ; chr19:g.39247459T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.372A>C	ENSP00000476098.1:p.Ter124Cys
ENST00000610963.1:c.371A>C	ENSP00000481371.1:p.Glu124Ala
ENST00000616270.4:c.422+9A>C	ENSP00000480679.1:n.422+9A>C
ENST00000634680.1:c.156A>C	ENSP00000489240.1:p.Ter52Cys
ENST00000634967.1:c.228A>C	ENSP00000489559.1:p.Ter76Cys
NR_074079.1:n.649A>C