Canonical Allele Identifier: CA2335423518
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247449C= , CM000681.2:g.39247449C= GRCh38
NC_000019.9:g.39738089C= , CM000681.1:g.39738089C= GRCh37
NC_000019.8:g.44429929C= NCBI36
NG_042193.1:g.2523G=
NG_055295.1:g.6408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.382G= ENSP00000476098.1:p.Ala128=
ENST00000610963.1:c.381G= ENSP00000481371.1:p.Arg127=
ENST00000616270.4:c.422+19G= ENSP00000480679.1:n.422+19G=
ENST00000634680.1:c.166G= ENSP00000489240.1:p.Ala56=
ENST00000634967.1:c.238G= ENSP00000489559.1:p.Ala80=
NR_074079.1:n.659G=