Canonical Allele Identifier: CA2335423658
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247715G= , CM000681.2:g.39247715G= GRCh38
NC_000019.9:g.39738355G= , CM000681.1:g.39738355G= GRCh37
NC_000019.8:g.44430195G= NCBI36
NG_042193.1:g.2257C=
NG_055295.1:g.6142C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.360C= ENSP00000476098.1:p.Gly120=
ENST00000610963.1:c.359C= ENSP00000481371.1:p.Ala120=
ENST00000616270.4:c.224-49C= ENSP00000480679.1:n.224-49C=
ENST00000634680.1:c.152-252C= ENSP00000489240.1:n.152-252C=
ENST00000634967.1:c.223+209C= ENSP00000489559.1:n.223+209C=
NR_074079.1:n.637C=