Canonical Allele Identifier: CA2335423795
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247968G= , CM000681.2:g.39247968G= GRCh38
NC_000019.9:g.39738608G= , CM000681.1:g.39738608G= GRCh37
NC_000019.8:g.44430448G= NCBI36
NG_042193.1:g.2004C=
NG_055295.1:g.5889C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.179C= ENSP00000476098.1:p.Ala60=
ENST00000610963.1:c.178C= ENSP00000481371.1:p.Arg60=
ENST00000616270.4:c.179C= ENSP00000480679.1:p.Ala60=
ENST00000634680.1:c.151+461C= ENSP00000489240.1:n.151+461C=
ENST00000634967.1:c.179C= ENSP00000489559.1:p.Ala60=
NR_074079.1:n.456C=