Canonical Allele Identifier: CA2335423692
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247781C= , CM000681.2:g.39247781C= GRCh38
NC_000019.9:g.39738421C= , CM000681.1:g.39738421C= GRCh37
NC_000019.8:g.44430261C= NCBI36
NG_042193.1:g.2191G=
NG_055295.1:g.6076G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.294G= ENSP00000476098.1:p.Pro98=
ENST00000610963.1:c.293G= ENSP00000481371.1:p.Arg98=
ENST00000616270.4:c.224-115G= ENSP00000480679.1:n.224-115G=
ENST00000634680.1:c.152-318G= ENSP00000489240.1:n.152-318G=
ENST00000634967.1:c.223+143G= ENSP00000489559.1:n.223+143G=
NR_074079.1:n.571G=