Canonical Allele Identifier: CA995767185
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs2074955456
gnomAD v3: 19-39247697-C-T
gnomAD v4: 19-39247697-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247697C>T , CM000681.2:g.39247697C>T GRCh38
NC_000019.9:g.39738337C>T , CM000681.1:g.39738337C>T GRCh37
NC_000019.8:g.44430177C>T NCBI36
NG_042193.1:g.2275G>A
NG_055295.1:g.6160G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+11G>A ENSP00000476098.1:n.367+11G>A
ENST00000610963.1:c.366+11G>A ENSP00000481371.1:n.366+11G>A
ENST00000616270.4:c.224-31G>A ENSP00000480679.1:n.224-31G>A
ENST00000634680.1:c.152-234G>A ENSP00000489240.1:n.152-234G>A
ENST00000634967.1:c.223+227G>A ENSP00000489559.1:n.223+227G>A
NR_074079.1:n.644+11G>A
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