Canonical Allele Identifier: CA405754984

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247445-C-A
• MyVariant Identifiers: chr19:g.39738085C>A (hg19) ; chr19:g.39247445C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247445C>A , CM000681.2:g.39247445C>A	GRCh38
NC_000019.9:g.39738085C>A , CM000681.1:g.39738085C>A	GRCh37
NC_000019.8:g.44429925C>A	NCBI36
NG_042193.1:g.2527G>T
NG_055295.1:g.6412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.386G>T	ENSP00000476098.1:p.Arg129Met
ENST00000610963.1:c.385G>T	ENSP00000481371.1:p.Gly129Cys
ENST00000616270.4:c.422+23G>T	ENSP00000480679.1:n.422+23G>T
ENST00000634680.1:c.170G>T	ENSP00000489240.1:p.Arg57Met
ENST00000634967.1:c.242G>T	ENSP00000489559.1:p.Arg81Met
NR_074079.1:n.663G>T