Canonical Allele Identifier: CA308189106

Gene: IFNL4

Linked Data

• dbSNP Id: rs577414432
• gnomAD v3: 19-39247588-G-T
• gnomAD v4: 19-39247588-G-T
• MyVariant Identifiers: chr19:g.39738228G>T (hg19) ; chr19:g.39247588G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247588G>T , CM000681.2:g.39247588G>T	GRCh38
NC_000019.9:g.39738228G>T , CM000681.1:g.39738228G>T	GRCh37
NC_000019.8:g.44430068G>T	NCBI36
NG_042193.1:g.2384C>A
NG_055295.1:g.6269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+120C>A	ENSP00000476098.1:n.367+120C>A
ENST00000610963.1:c.366+120C>A	ENSP00000481371.1:n.366+120C>A
ENST00000616270.4:c.302C>A	ENSP00000480679.1:p.Thr101Asn
ENST00000634680.1:c.152-125C>A	ENSP00000489240.1:n.152-125C>A
ENST00000634967.1:c.224-125C>A	ENSP00000489559.1:n.224-125C>A
NR_074079.1:n.644+120C>A