Canonical Allele Identifier: CA405755057

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247463-G-T
• MyVariant Identifiers: chr19:g.39738103G>T (hg19) ; chr19:g.39247463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247463G>T , CM000681.2:g.39247463G>T	GRCh38
NC_000019.9:g.39738103G>T , CM000681.1:g.39738103G>T	GRCh37
NC_000019.8:g.44429943G>T	NCBI36
NG_042193.1:g.2509C>A
NG_055295.1:g.6394C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368C>A	ENSP00000476098.1:p.Pro123His
ENST00000610963.1:c.367C>A	ENSP00000481371.1:p.Leu123Ile
ENST00000616270.4:c.422+5C>A	ENSP00000480679.1:n.422+5C>A
ENST00000634680.1:c.152C>A	ENSP00000489240.1:p.Pro51His
ENST00000634967.1:c.224C>A	ENSP00000489559.1:p.Ala75Asp
NR_074079.1:n.645C>A