Canonical Allele Identifier: CA995767147

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074955155
• gnomAD v3: 19-39247653-AGGAT-A
• gnomAD v4: 19-39247653-AGGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247655_39247658del , CM000681.2:g.39247655_39247658del	GRCh38
NC_000019.9:g.39738295_39738298del , CM000681.1:g.39738295_39738298del	GRCh37
NC_000019.8:g.44430135_44430138del	NCBI36
NG_042193.1:g.2315_2318del
NG_055295.1:g.6200_6203del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+51_367+54del	ENSP00000476098.1:n.367+51_367+54del
ENST00000610963.1:c.366+51_366+54del	ENSP00000481371.1:n.366+51_366+54del
ENST00000616270.4:c.233_236del	ENSP00000480679.1:p.His78LeufsTer16
ENST00000634680.1:c.152-194_152-191del	ENSP00000489240.1:n.152-194_152-191del
ENST00000634967.1:c.224-194_224-191del	ENSP00000489559.1:n.224-194_224-191del
NR_074079.1:n.644+51_644+54del