ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756841
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247973-C-A
MyVariant Identifiers:
chr19:g.39738613C>A (hg19)
chr19:g.39247973C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247973C>A , CM000681.2:g.39247973C>A
GRCh38
NC_000019.9:g.39738613C>A , CM000681.1:g.39738613C>A
GRCh37
NC_000019.8:g.44430453C>A
NCBI36
NG_042193.1:g.1999G>T
NG_055295.1:g.5884G>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000606380.2:c.174G>T
ENSP00000476098.1:p.Gly58=
ENST00000610963.1:c.173G>T
ENSP00000481371.1:p.Gly58Val
ENST00000616270.4:c.174G>T
ENSP00000480679.1:p.Gly58=
ENST00000634680.1:c.151+456G>T
ENSP00000489240.1:n.151+456G>T
ENST00000634967.1:c.174G>T
ENSP00000489559.1:p.Gly58=
NR_074079.1:n.451G>T
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