Canonical Allele Identifier: CA2335423665
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247726C= , CM000681.2:g.39247726C= GRCh38
NC_000019.9:g.39738366C= , CM000681.1:g.39738366C= GRCh37
NC_000019.8:g.44430206C= NCBI36
NG_042193.1:g.2246G=
NG_055295.1:g.6131G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.349G= ENSP00000476098.1:p.Glu117=
ENST00000610963.1:c.348G= ENSP00000481371.1:p.Gly116=
ENST00000616270.4:c.224-60G= ENSP00000480679.1:n.224-60G=
ENST00000634680.1:c.152-263G= ENSP00000489240.1:n.152-263G=
ENST00000634967.1:c.223+198G= ENSP00000489559.1:n.223+198G=
NR_074079.1:n.626G=