Canonical Allele Identifier: CA2582150882

Gene: IFNL4

Linked Data

• gnomAD v3: 19-39247638-C-CT
• gnomAD v4: 19-39247638-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247639dup , CM000681.2:g.39247639dup	GRCh38
NC_000019.9:g.39738279dup , CM000681.1:g.39738279dup	GRCh37
NC_000019.8:g.44430119dup	NCBI36
NG_042193.1:g.2333dup
NG_055295.1:g.6218dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+69dup	ENSP00000476098.1:n.367+69dup
ENST00000610963.1:c.366+69dup	ENSP00000481371.1:n.366+69dup
ENST00000616270.4:c.251dup	ENSP00000480679.1:p.Pro85AlafsTer26
ENST00000634680.1:c.152-176dup	ENSP00000489240.1:n.152-176dup
ENST00000634967.1:c.224-176dup	ENSP00000489559.1:n.224-176dup
NR_074079.1:n.644+69dup