Canonical Allele Identifier: CA405755671

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247603-T-G
• MyVariant Identifiers: chr19:g.39738243T>G (hg19) ; chr19:g.39247603T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247603T>G , CM000681.2:g.39247603T>G	GRCh38
NC_000019.9:g.39738243T>G , CM000681.1:g.39738243T>G	GRCh37
NC_000019.8:g.44430083T>G	NCBI36
NG_042193.1:g.2369A>C
NG_055295.1:g.6254A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+105A>C	ENSP00000476098.1:n.367+105A>C
ENST00000610963.1:c.366+105A>C	ENSP00000481371.1:n.366+105A>C
ENST00000616270.4:c.287A>C	ENSP00000480679.1:p.Glu96Ala
ENST00000634680.1:c.152-140A>C	ENSP00000489240.1:n.152-140A>C
ENST00000634967.1:c.224-140A>C	ENSP00000489559.1:n.224-140A>C
NR_074079.1:n.644+105A>C