ClinGen Allele Registry
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Canonical Allele Identifier:
CA405755669
Gene: IFNL4
HGNC
NCBI
Linked Data
dbSNP Id:
rs1467674178
gnomAD v2:
19-39738243-T-C
gnomAD v3:
19-39247603-T-C
gnomAD v4:
19-39247603-T-C
MyVariant Identifiers:
chr19:g.39738243T>C (hg19)
chr19:g.39247603T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247603T>C , CM000681.2:g.39247603T>C
GRCh38
NC_000019.9:g.39738243T>C , CM000681.1:g.39738243T>C
GRCh37
NC_000019.8:g.44430083T>C
NCBI36
NG_042193.1:g.2369A>G
NG_055295.1:g.6254A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.367+105A>G
ENSP00000476098.1:n.367+105A>G
ENST00000610963.1:c.366+105A>G
ENSP00000481371.1:n.366+105A>G
ENST00000616270.4:c.287A>G
ENSP00000480679.1:p.Glu96Gly
ENST00000634680.1:c.152-140A>G
ENSP00000489240.1:n.152-140A>G
ENST00000634967.1:c.224-140A>G
ENSP00000489559.1:n.224-140A>G
NR_074079.1:n.644+105A>G
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