Canonical Allele Identifier: CA2335423672
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247741C= , CM000681.2:g.39247741C= GRCh38
NC_000019.9:g.39738381C= , CM000681.1:g.39738381C= GRCh37
NC_000019.8:g.44430221C= NCBI36
NG_042193.1:g.2231G=
NG_055295.1:g.6116G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.334G= ENSP00000476098.1:p.Ala112=
ENST00000610963.1:c.333G= ENSP00000481371.1:p.Leu111=
ENST00000616270.4:c.224-75G= ENSP00000480679.1:n.224-75G=
ENST00000634680.1:c.152-278G= ENSP00000489240.1:n.152-278G=
ENST00000634967.1:c.223+183G= ENSP00000489559.1:n.223+183G=
NR_074079.1:n.611G=