ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756866
Gene: IFNL4
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr19:g.39738618G>C (hg19)
chr19:g.39247978G>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247978G>C , CM000681.2:g.39247978G>C
GRCh38
NC_000019.9:g.39738618G>C , CM000681.1:g.39738618G>C
GRCh37
NC_000019.8:g.44430458G>C
NCBI36
NG_042193.1:g.1994C>G
NG_055295.1:g.5879C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.169C>G
ENSP00000476098.1:p.Leu57Val
ENST00000610963.1:c.168C>G
ENSP00000481371.1:p.Ser56Arg
ENST00000616270.4:c.169C>G
ENSP00000480679.1:p.Leu57Val
ENST00000634680.1:c.151+451C>G
ENSP00000489240.1:n.151+451C>G
ENST00000634967.1:c.169C>G
ENSP00000489559.1:p.Leu57Val
NR_074079.1:n.446C>G
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