Canonical Allele Identifier: CA2335423796
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247971G= , CM000681.2:g.39247971G= GRCh38
NC_000019.9:g.39738611G= , CM000681.1:g.39738611G= GRCh37
NC_000019.8:g.44430451G= NCBI36
NG_042193.1:g.2001C=
NG_055295.1:g.5886C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.176C= ENSP00000476098.1:p.Ala59=
ENST00000610963.1:c.175C= ENSP00000481371.1:p.Gln59=
ENST00000616270.4:c.176C= ENSP00000480679.1:p.Ala59=
ENST00000634680.1:c.151+458C= ENSP00000489240.1:n.151+458C=
ENST00000634967.1:c.176C= ENSP00000489559.1:p.Ala59=
NR_074079.1:n.453C=