Canonical Allele Identifier: CA2335423696
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs2074956096

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247784del , CM000681.2:g.39247784del GRCh38
NC_000019.9:g.39738424del , CM000681.1:g.39738424del GRCh37
NC_000019.8:g.44430264del NCBI36
NG_042193.1:g.2188del
NG_055295.1:g.6073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.291del ENSP00000476098.1:p.Pro98ArgfsTer?
ENST00000610963.1:c.290del ENSP00000481371.1:p.His97ProfsTer?
ENST00000616270.4:c.224-118del ENSP00000480679.1:n.224-118del
ENST00000634680.1:c.152-321del ENSP00000489240.1:n.152-321del
ENST00000634967.1:c.223+140del ENSP00000489559.1:n.223+140del
NR_074079.1:n.568del