Canonical Allele Identifier: CA405755649

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247599-T-G
• MyVariant Identifiers: chr19:g.39738239T>G (hg19) ; chr19:g.39247599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247599T>G , CM000681.2:g.39247599T>G	GRCh38
NC_000019.9:g.39738239T>G , CM000681.1:g.39738239T>G	GRCh37
NC_000019.8:g.44430079T>G	NCBI36
NG_042193.1:g.2373A>C
NG_055295.1:g.6258A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+109A>C	ENSP00000476098.1:n.367+109A>C
ENST00000610963.1:c.366+109A>C	ENSP00000481371.1:n.366+109A>C
ENST00000616270.4:c.291A>C	ENSP00000480679.1:p.Lys97Asn
ENST00000634680.1:c.152-136A>C	ENSP00000489240.1:n.152-136A>C
ENST00000634967.1:c.224-136A>C	ENSP00000489559.1:n.224-136A>C
NR_074079.1:n.644+109A>C