Canonical Allele Identifier: CA882118771

Gene: IFNL4

Linked Data

• dbSNP Id: rs1162217255
• MyVariant Identifiers: chr19:g.39738170_39738178del (hg19) ; chr19:g.39247530_39247538del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247533_39247541del , CM000681.2:g.39247533_39247541del	GRCh38
NC_000019.9:g.39738173_39738181del , CM000681.1:g.39738173_39738181del	GRCh37
NC_000019.8:g.44430013_44430021del	NCBI36
NG_042193.1:g.2434_2442del
NG_055295.1:g.6319_6327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-75_368-67del	ENSP00000476098.1:n.368-75_368-67del
ENST00000610963.1:c.367-75_367-67del	ENSP00000481371.1:n.367-75_367-67del
ENST00000616270.4:c.352_360del	ENSP00000480679.1:p.Trp118_Gly120del
ENST00000634680.1:c.152-75_152-67del	ENSP00000489240.1:n.152-75_152-67del
ENST00000634967.1:c.224-75_224-67del	ENSP00000489559.1:n.224-75_224-67del
NR_074079.1:n.645-75_645-67del