Canonical Allele Identifier: CA2335423871
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248116G= , CM000681.2:g.39248116G= GRCh38
NC_000019.9:g.39738756G= , CM000681.1:g.39738756G= GRCh37
NC_000019.8:g.44430596G= NCBI36
NG_042193.1:g.1856C=
NG_055295.1:g.5741C=

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-121C= ENSP00000476098.1:n.152-121C=
ENST00000610963.1:c.151-121C= ENSP00000481371.1:n.151-121C=
ENST00000616270.4:c.152-121C= ENSP00000480679.1:n.152-121C=
ENST00000634680.1:c.151+313C= ENSP00000489240.1:n.151+313C=
ENST00000634967.1:c.152-121C= ENSP00000489559.1:n.152-121C=
NR_074079.1:n.429-121C=