Canonical Allele Identifier: CA2335423951
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248261C= , CM000681.2:g.39248261C= GRCh38
NC_000019.9:g.39738901C= , CM000681.1:g.39738901C= GRCh37
NC_000019.8:g.44430741C= NCBI36
NG_042193.1:g.1711G=
NG_055295.1:g.5596G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+168G= ENSP00000476098.1:n.151+168G=
ENST00000610963.1:c.150+168G= ENSP00000481371.1:n.150+168G=
ENST00000616270.4:c.151+168G= ENSP00000480679.1:n.151+168G=
ENST00000634680.1:c.151+168G= ENSP00000489240.1:n.151+168G=
ENST00000634967.1:c.151+168G= ENSP00000489559.1:n.151+168G=
NR_074079.1:n.428+168G=