ClinGen Allele Registry
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Canonical Allele Identifier:
CA405756834
Gene: IFNL4
HGNC
NCBI
Linked Data
gnomAD v4:
19-39247971-G-T
MyVariant Identifiers:
chr19:g.39738611G>T (hg19)
chr19:g.39247971G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247971G>T , CM000681.2:g.39247971G>T
GRCh38
NC_000019.9:g.39738611G>T , CM000681.1:g.39738611G>T
GRCh37
NC_000019.8:g.44430451G>T
NCBI36
NG_042193.1:g.2001C>A
NG_055295.1:g.5886C>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000606380.2:c.176C>A
ENSP00000476098.1:p.Ala59Glu
ENST00000610963.1:c.175C>A
ENSP00000481371.1:p.Gln59Lys
ENST00000616270.4:c.176C>A
ENSP00000480679.1:p.Ala59Glu
ENST00000634680.1:c.151+458C>A
ENSP00000489240.1:n.151+458C>A
ENST00000634967.1:c.176C>A
ENSP00000489559.1:p.Ala59Glu
NR_074079.1:n.453C>A
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