Canonical Allele Identifier: CA633069305
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1184695764
gnomAD v2: 19-39738311-CG-C
gnomAD v3: 19-39247671-CG-C
gnomAD v4: 19-39247671-CG-C
MyVariant Identifiers: chr19:g.39738312del (hg19) chr19:g.39247672del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247676del , CM000681.2:g.39247676del GRCh38
NC_000019.9:g.39738316del , CM000681.1:g.39738316del GRCh37
NC_000019.8:g.44430156del NCBI36
NG_042193.1:g.2300del
NG_055295.1:g.6185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+36del ENSP00000476098.1:n.367+36del
ENST00000610963.1:c.366+36del ENSP00000481371.1:n.366+36del
ENST00000616270.4:c.224-6del ENSP00000480679.1:n.224-6del
ENST00000634680.1:c.152-209del ENSP00000489240.1:n.152-209del
ENST00000634967.1:c.224-209del ENSP00000489559.1:n.224-209del
NR_074079.1:n.644+36del
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