Canonical Allele Identifier: CA2335423519
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247450C= , CM000681.2:g.39247450C= GRCh38
NC_000019.9:g.39738090C= , CM000681.1:g.39738090C= GRCh37
NC_000019.8:g.44429930C= NCBI36
NG_042193.1:g.2522G=
NG_055295.1:g.6407G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.381G= ENSP00000476098.1:p.Thr127=
ENST00000610963.1:c.380G= ENSP00000481371.1:p.Arg127=
ENST00000616270.4:c.422+18G= ENSP00000480679.1:n.422+18G=
ENST00000634680.1:c.165G= ENSP00000489240.1:p.Thr55=
ENST00000634967.1:c.237G= ENSP00000489559.1:p.Thr79=
NR_074079.1:n.658G=