Canonical Allele Identifier: CA10576188
Gene: IFNL4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225949
dbSNP Id: rs12979860

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248147C>T , CM000681.2:g.39248147C>T GRCh38
NC_000019.9:g.39738787C>T , CM000681.1:g.39738787C>T GRCh37
NC_000019.8:g.44430627C>T NCBI36
NG_042193.1:g.1825G>A
NG_055295.1:g.5710G>A

Transcript Alleles

HGVS Amino-acid change
NR_074079.1:n.429-152G>A
ENST00000606380.2:c.152-152G>A ENSP00000476098.1:p.=
ENST00000610963.1:c.151-152G>A ENSP00000481371.1:p.=
ENST00000616270.4:c.152-152G>A ENSP00000480679.1:p.=
ENST00000634680.1:c.151+282G>A ENSP00000489240.1:p.=
ENST00000634967.1:c.152-152G>A ENSP00000489559.1:p.=