Canonical Allele Identifier: CA405756925

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247989-C-A
• MyVariant Identifiers: chr19:g.39738629C>A (hg19) ; chr19:g.39247989C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247989C>A , CM000681.2:g.39247989C>A	GRCh38
NC_000019.9:g.39738629C>A , CM000681.1:g.39738629C>A	GRCh37
NC_000019.8:g.44430469C>A	NCBI36
NG_042193.1:g.1983G>T
NG_055295.1:g.5868G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.158G>T	ENSP00000476098.1:p.Arg53Ile
ENST00000610963.1:c.157G>T	ENSP00000481371.1:p.Glu53Ter
ENST00000616270.4:c.158G>T	ENSP00000480679.1:p.Arg53Ile
ENST00000634680.1:c.151+440G>T	ENSP00000489240.1:n.151+440G>T
ENST00000634967.1:c.158G>T	ENSP00000489559.1:p.Arg53Ile
NR_074079.1:n.435G>T