Canonical Allele Identifier: CA2584994916
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39248105-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248105T>C , CM000681.2:g.39248105T>C GRCh38
NC_000019.9:g.39738745T>C , CM000681.1:g.39738745T>C GRCh37
NC_000019.8:g.44430585T>C NCBI36
NG_042193.1:g.1867A>G
NG_055295.1:g.5752A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-110A>G ENSP00000476098.1:n.152-110A>G
ENST00000610963.1:c.151-110A>G ENSP00000481371.1:n.151-110A>G
ENST00000616270.4:c.152-110A>G ENSP00000480679.1:n.152-110A>G
ENST00000634680.1:c.151+324A>G ENSP00000489240.1:n.151+324A>G
ENST00000634967.1:c.152-110A>G ENSP00000489559.1:n.152-110A>G
NR_074079.1:n.429-110A>G
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