Canonical Allele Identifier: CA2335423698
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247785G= , CM000681.2:g.39247785G= GRCh38
NC_000019.9:g.39738425G= , CM000681.1:g.39738425G= GRCh37
NC_000019.8:g.44430265G= NCBI36
NG_042193.1:g.2187C=
NG_055295.1:g.6072C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.290C= ENSP00000476098.1:p.Ala97=
ENST00000610963.1:c.289C= ENSP00000481371.1:p.His97=
ENST00000616270.4:c.224-119C= ENSP00000480679.1:n.224-119C=
ENST00000634680.1:c.152-322C= ENSP00000489240.1:n.152-322C=
ENST00000634967.1:c.223+139C= ENSP00000489559.1:n.223+139C=
NR_074079.1:n.567C=