Canonical Allele Identifier: CA2335423805
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247994T= , CM000681.2:g.39247994T= GRCh38
NC_000019.9:g.39738634T= , CM000681.1:g.39738634T= GRCh37
NC_000019.8:g.44430474T= NCBI36
NG_042193.1:g.1978A=
NG_055295.1:g.5863A=

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.153A= ENSP00000476098.1:p.Arg51=
ENST00000610963.1:c.152A= ENSP00000481371.1:p.Glu51=
ENST00000616270.4:c.153A= ENSP00000480679.1:p.Arg51=
ENST00000634680.1:c.151+435A= ENSP00000489240.1:n.151+435A=
ENST00000634967.1:c.153A= ENSP00000489559.1:p.Arg51=
NR_074079.1:n.430A=