Canonical Allele Identifier: CA633069239
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1261483207
gnomAD v2: 19-39738129-GA-G
gnomAD v4: 19-39247489-GA-G
MyVariant Identifiers: chr19:g.39738130del (hg19) chr19:g.39247490del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247493del , CM000681.2:g.39247493del GRCh38
NC_000019.9:g.39738133del , CM000681.1:g.39738133del GRCh37
NC_000019.8:g.44429973del NCBI36
NG_042193.1:g.2482del
NG_055295.1:g.6367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.368-27del ENSP00000476098.1:n.368-27del
ENST00000610963.1:c.367-27del ENSP00000481371.1:n.367-27del
ENST00000616270.4:c.400del ENSP00000480679.1:p.Ser134ProfsTer14
ENST00000634680.1:c.152-27del ENSP00000489240.1:n.152-27del
ENST00000634967.1:c.224-27del ENSP00000489559.1:n.224-27del
NR_074079.1:n.645-27del
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