ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756958
Gene: IFNL4
HGNC
NCBI
Linked Data
dbSNP Id:
rs1475349409
gnomAD v3:
19-39247995-C-A
gnomAD v4:
19-39247995-C-A
MyVariant Identifiers:
chr19:g.39738635C>A (hg19)
chr19:g.39247995C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247995C>A , CM000681.2:g.39247995C>A
GRCh38
NC_000019.9:g.39738635C>A , CM000681.1:g.39738635C>A
GRCh37
NC_000019.8:g.44430475C>A
NCBI36
NG_042193.1:g.1977G>T
NG_055295.1:g.5862G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.152G>T
ENSP00000476098.1:p.Arg51Leu
ENST00000610963.1:c.151G>T
ENSP00000481371.1:p.Glu51Ter
ENST00000616270.4:c.152G>T
ENSP00000480679.1:p.Arg51Leu
ENST00000634680.1:c.151+434G>T
ENSP00000489240.1:n.151+434G>T
ENST00000634967.1:c.152G>T
ENSP00000489559.1:p.Arg51Leu
NR_074079.1:n.429G>T
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