Canonical Allele Identifier: CA405755605

Gene: IFNL4

Linked Data

• dbSNP Id: rs1399185229
• gnomAD v3: 19-39247589-T-G
• gnomAD v4: 19-39247589-T-G
• MyVariant Identifiers: chr19:g.39738229T>G (hg19) ; chr19:g.39247589T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247589T>G , CM000681.2:g.39247589T>G	GRCh38
NC_000019.9:g.39738229T>G , CM000681.1:g.39738229T>G	GRCh37
NC_000019.8:g.44430069T>G	NCBI36
NG_042193.1:g.2383A>C
NG_055295.1:g.6268A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+119A>C	ENSP00000476098.1:n.367+119A>C
ENST00000610963.1:c.366+119A>C	ENSP00000481371.1:n.366+119A>C
ENST00000616270.4:c.301A>C	ENSP00000480679.1:p.Thr101Pro
ENST00000634680.1:c.152-126A>C	ENSP00000489240.1:n.152-126A>C
ENST00000634967.1:c.224-126A>C	ENSP00000489559.1:n.224-126A>C
NR_074079.1:n.644+119A>C