Canonical Allele Identifier: CA2335423691
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247780G= , CM000681.2:g.39247780G= GRCh38
NC_000019.9:g.39738420G= , CM000681.1:g.39738420G= GRCh37
NC_000019.8:g.44430260G= NCBI36
NG_042193.1:g.2192C=
NG_055295.1:g.6077C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.295C= ENSP00000476098.1:p.Leu99=
ENST00000610963.1:c.294C= ENSP00000481371.1:p.Arg98=
ENST00000616270.4:c.224-114C= ENSP00000480679.1:n.224-114C=
ENST00000634680.1:c.152-317C= ENSP00000489240.1:n.152-317C=
ENST00000634967.1:c.223+144C= ENSP00000489559.1:n.223+144C=
NR_074079.1:n.572C=