Canonical Allele Identifier: CA405755025

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247456-A-C
• MyVariant Identifiers: chr19:g.39738096A>C (hg19) ; chr19:g.39247456A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247456A>C , CM000681.2:g.39247456A>C	GRCh38
NC_000019.9:g.39738096A>C , CM000681.1:g.39738096A>C	GRCh37
NC_000019.8:g.44429936A>C	NCBI36
NG_042193.1:g.2516T>G
NG_055295.1:g.6401T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.375T>G	ENSP00000476098.1:p.Ala125=
ENST00000610963.1:c.374T>G	ENSP00000481371.1:p.Leu125Arg
ENST00000616270.4:c.422+12T>G	ENSP00000480679.1:n.422+12T>G
ENST00000634680.1:c.159T>G	ENSP00000489240.1:p.Ala53=
ENST00000634967.1:c.231T>G	ENSP00000489559.1:p.Ala77=
NR_074079.1:n.652T>G