Canonical Allele Identifier: CA405755032

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247457-G-T
• MyVariant Identifiers: chr19:g.39738097G>T (hg19) ; chr19:g.39247457G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247457G>T , CM000681.2:g.39247457G>T	GRCh38
NC_000019.9:g.39738097G>T , CM000681.1:g.39738097G>T	GRCh37
NC_000019.8:g.44429937G>T	NCBI36
NG_042193.1:g.2515C>A
NG_055295.1:g.6400C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.374C>A	ENSP00000476098.1:p.Ala125Asp
ENST00000610963.1:c.373C>A	ENSP00000481371.1:p.Leu125Met
ENST00000616270.4:c.422+11C>A	ENSP00000480679.1:n.422+11C>A
ENST00000634680.1:c.158C>A	ENSP00000489240.1:p.Ala53Asp
ENST00000634967.1:c.230C>A	ENSP00000489559.1:p.Ala77Asp
NR_074079.1:n.651C>A