Canonical Allele Identifier: CA995804625

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074954271
• gnomAD v3: 19-39247478-TG-T
• gnomAD v4: 19-39247478-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247479del , CM000681.2:g.39247479del	GRCh38
NC_000019.9:g.39738119del , CM000681.1:g.39738119del	GRCh37
NC_000019.8:g.44429959del	NCBI36
NG_042193.1:g.2493del
NG_055295.1:g.6378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-16del	ENSP00000476098.1:n.368-16del
ENST00000610963.1:c.367-16del	ENSP00000481371.1:n.367-16del
ENST00000616270.4:c.411del	ENSP00000480679.1:p.Met138CysfsTer10
ENST00000634680.1:c.152-16del	ENSP00000489240.1:n.152-16del
ENST00000634967.1:c.224-16del	ENSP00000489559.1:n.224-16del
NR_074079.1:n.645-16del