Canonical Allele Identifier: CA405754981

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247444-C-T
• MyVariant Identifiers: chr19:g.39738084C>T (hg19) ; chr19:g.39247444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247444C>T , CM000681.2:g.39247444C>T	GRCh38
NC_000019.9:g.39738084C>T , CM000681.1:g.39738084C>T	GRCh37
NC_000019.8:g.44429924C>T	NCBI36
NG_042193.1:g.2528G>A
NG_055295.1:g.6413G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.387G>A	ENSP00000476098.1:p.Arg129=
ENST00000610963.1:c.386G>A	ENSP00000481371.1:p.Gly129Asp
ENST00000616270.4:c.422+24G>A	ENSP00000480679.1:n.422+24G>A
ENST00000634680.1:c.171G>A	ENSP00000489240.1:p.Arg57=
ENST00000634967.1:c.243G>A	ENSP00000489559.1:p.Arg81=
NR_074079.1:n.664G>A