Canonical Allele Identifier: CA405756283

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247787-A-G
• MyVariant Identifiers: chr19:g.39738427A>G (hg19) ; chr19:g.39247787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247787A>G , CM000681.2:g.39247787A>G	GRCh38
NC_000019.9:g.39738427A>G , CM000681.1:g.39738427A>G	GRCh37
NC_000019.8:g.44430267A>G	NCBI36
NG_042193.1:g.2185T>C
NG_055295.1:g.6070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.288T>C	ENSP00000476098.1:p.Pro96=
ENST00000610963.1:c.287T>C	ENSP00000481371.1:p.Leu96Pro
ENST00000616270.4:c.224-121T>C	ENSP00000480679.1:n.224-121T>C
ENST00000634680.1:c.152-324T>C	ENSP00000489240.1:n.152-324T>C
ENST00000634967.1:c.223+137T>C	ENSP00000489559.1:n.223+137T>C
NR_074079.1:n.565T>C