ClinGen Allele Registry
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Canonical Allele Identifier:
CA2584994646
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247436-TG-T
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247438del , CM000681.2:g.39247438del
GRCh38
NC_000019.9:g.39738078del , CM000681.1:g.39738078del
GRCh37
NC_000019.8:g.44429918del
NCBI36
NG_042193.1:g.2535del
NG_055295.1:g.6420del
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.394del
ENSP00000476098.1:p.Gln132ArgfsTer?
ENST00000610963.1:c.393del
ENSP00000481371.1:p.Arg132GlyfsTer?
ENST00000616270.4:c.422+31del
ENSP00000480679.1:n.422+31del
ENST00000634680.1:c.178del
ENSP00000489240.1:p.Gln60ArgfsTer?
ENST00000634967.1:c.250del
ENSP00000489559.1:p.Gln84ArgfsTer?
NR_074079.1:n.671del
Search 100 bp 5'
Search 100 bp 3'