Canonical Allele Identifier: CA633069308
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1354288465
gnomAD v2: 19-39738346-AC-A
gnomAD v3: 19-39247706-AC-A
gnomAD v4: 19-39247706-AC-A
MyVariant Identifiers: chr19:g.39738347del (hg19) chr19:g.39247707del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247707del , CM000681.2:g.39247707del GRCh38
NC_000019.9:g.39738347del , CM000681.1:g.39738347del GRCh37
NC_000019.8:g.44430187del NCBI36
NG_042193.1:g.2265del
NG_055295.1:g.6150del

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+1del ENSP00000476098.1:n.367+1del
ENST00000610963.1:c.366+1del ENSP00000481371.1:n.366+1del
ENST00000616270.4:c.224-41del ENSP00000480679.1:n.224-41del
ENST00000634680.1:c.152-244del ENSP00000489240.1:n.152-244del
ENST00000634967.1:c.223+217del ENSP00000489559.1:n.223+217del
NR_074079.1:n.644+1del
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