Canonical Allele Identifier: CA2584994725

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247687-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247687_39247688insA , CM000681.2:g.39247687_39247688insA	GRCh38
NC_000019.9:g.39738327_39738328insA , CM000681.1:g.39738327_39738328insA	GRCh37
NC_000019.8:g.44430167_44430168insA	NCBI36
NG_042193.1:g.2284_2285insT
NG_055295.1:g.6169_6170insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+20_367+21insT	ENSP00000476098.1:n.367+20_367+21insT
ENST00000610963.1:c.366+20_366+21insT	ENSP00000481371.1:n.366+20_366+21insT
ENST00000616270.4:c.224-22_224-21insT	ENSP00000480679.1:n.224-22_224-21insT
ENST00000634680.1:c.152-225_152-224insT	ENSP00000489240.1:n.152-225_152-224insT
ENST00000634967.1:c.224-225_224-224insT	ENSP00000489559.1:n.224-225_224-224insT
NR_074079.1:n.644+20_644+21insT