Canonical Allele Identifier: CA633069280

Gene: IFNL4

Linked Data

• dbSNP Id: rs1294503020
• gnomAD v2: 19-39738226-C-CTG
• gnomAD v3: 19-39247586-C-CTG
• gnomAD v4: 19-39247586-C-CTG
• MyVariant Identifiers: chr19:g.39738226_39738227insTG (hg19) ; chr19:g.39247586_39247587insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247586_39247587insTG , CM000681.2:g.39247586_39247587insTG	GRCh38
NC_000019.9:g.39738226_39738227insTG , CM000681.1:g.39738226_39738227insTG	GRCh37
NC_000019.8:g.44430066_44430067insTG	NCBI36
NG_042193.1:g.2385_2386insCA
NG_055295.1:g.6270_6271insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+121_368-123insCA	ENSP00000476098.1:n.367+121_368-123insCA
ENST00000610963.1:c.366+121_367-123insCA	ENSP00000481371.1:n.366+121_367-123insCA
ENST00000616270.4:c.303_304insCA	ENSP00000480679.1:p.Gly102GlnfsTer?
ENST00000634680.1:c.152-124_152-123insCA	ENSP00000489240.1:n.152-124_152-123insCA
ENST00000634967.1:c.224-124_224-123insCA	ENSP00000489559.1:n.224-124_224-123insCA
NR_074079.1:n.644+121_645-123insCA