Canonical Allele Identifier: CA405755053

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247462-A-G
• MyVariant Identifiers: chr19:g.39738102A>G (hg19) ; chr19:g.39247462A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247462A>G , CM000681.2:g.39247462A>G	GRCh38
NC_000019.9:g.39738102A>G , CM000681.1:g.39738102A>G	GRCh37
NC_000019.8:g.44429942A>G	NCBI36
NG_042193.1:g.2510T>C
NG_055295.1:g.6395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.369T>C	ENSP00000476098.1:p.Pro123=
ENST00000610963.1:c.368T>C	ENSP00000481371.1:p.Leu123Pro
ENST00000616270.4:c.422+6T>C	ENSP00000480679.1:n.422+6T>C
ENST00000634680.1:c.153T>C	ENSP00000489240.1:p.Pro51=
ENST00000634967.1:c.225T>C	ENSP00000489559.1:p.Ala75=
NR_074079.1:n.646T>C