ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756812
Gene: IFNL4
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr19:g.39738607C>A (hg19)
chr19:g.39247967C>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247967C>A , CM000681.2:g.39247967C>A
GRCh38
NC_000019.9:g.39738607C>A , CM000681.1:g.39738607C>A
GRCh37
NC_000019.8:g.44430447C>A
NCBI36
NG_042193.1:g.2005G>T
NG_055295.1:g.5890G>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000606380.2:c.180G>T
ENSP00000476098.1:p.Ala60=
ENST00000610963.1:c.179G>T
ENSP00000481371.1:p.Arg60Leu
ENST00000616270.4:c.180G>T
ENSP00000480679.1:p.Ala60=
ENST00000634680.1:c.151+462G>T
ENSP00000489240.1:n.151+462G>T
ENST00000634967.1:c.180G>T
ENSP00000489559.1:p.Ala60=
NR_074079.1:n.457G>T
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