Canonical Allele Identifier: CA308189613
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs956243689

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248118del , CM000681.2:g.39248118del GRCh38
NC_000019.9:g.39738758del , CM000681.1:g.39738758del GRCh37
NC_000019.8:g.44430598del NCBI36
NG_042193.1:g.1854del
NG_055295.1:g.5739del

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-123del ENSP00000476098.1:n.152-123del
ENST00000610963.1:c.151-123del ENSP00000481371.1:n.151-123del
ENST00000616270.4:c.152-123del ENSP00000480679.1:n.152-123del
ENST00000634680.1:c.151+311del ENSP00000489240.1:n.151+311del
ENST00000634967.1:c.152-123del ENSP00000489559.1:n.152-123del
NR_074079.1:n.429-123del