Canonical Allele Identifier: CA2335423619
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247657T= , CM000681.2:g.39247657T= GRCh38
NC_000019.9:g.39738297T= , CM000681.1:g.39738297T= GRCh37
NC_000019.8:g.44430137T= NCBI36
NG_042193.1:g.2315A=
NG_055295.1:g.6200A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+51A= ENSP00000476098.1:n.367+51A=
ENST00000610963.1:c.366+51A= ENSP00000481371.1:n.366+51A=
ENST00000616270.4:c.233A= ENSP00000480679.1:p.His78=
ENST00000634680.1:c.152-194A= ENSP00000489240.1:n.152-194A=
ENST00000634967.1:c.224-194A= ENSP00000489559.1:n.224-194A=
NR_074079.1:n.644+51A=