Canonical Allele Identifier: CA882118738

Gene: IFNL4

Linked Data

• dbSNP Id: rs1439536289
• gnomAD v3: 19-39247510-CCT-C
• gnomAD v4: 19-39247510-CCT-C
• MyVariant Identifiers: chr19:g.39738151_39738152del (hg19) ; chr19:g.39247511_39247512del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247515_39247516del , CM000681.2:g.39247515_39247516del	GRCh38
NC_000019.9:g.39738155_39738156del , CM000681.1:g.39738155_39738156del	GRCh37
NC_000019.8:g.44429995_44429996del	NCBI36
NG_042193.1:g.2460_2461del
NG_055295.1:g.6345_6346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-49_368-48del	ENSP00000476098.1:n.368-49_368-48del
ENST00000610963.1:c.367-49_367-48del	ENSP00000481371.1:n.367-49_367-48del
ENST00000616270.4:c.378_379del	ENSP00000480679.1:p.Ala128PhefsTer?
ENST00000634680.1:c.152-49_152-48del	ENSP00000489240.1:n.152-49_152-48del
ENST00000634967.1:c.224-49_224-48del	ENSP00000489559.1:n.224-49_224-48del
NR_074079.1:n.645-49_645-48del