Canonical Allele Identifier: CA2584994678
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247563-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247563A>G , CM000681.2:g.39247563A>G GRCh38
NC_000019.9:g.39738203A>G , CM000681.1:g.39738203A>G GRCh37
NC_000019.8:g.44430043A>G NCBI36
NG_042193.1:g.2409T>C
NG_055295.1:g.6294T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.368-100T>C ENSP00000476098.1:n.368-100T>C
ENST00000610963.1:c.367-100T>C ENSP00000481371.1:n.367-100T>C
ENST00000616270.4:c.327T>C ENSP00000480679.1:p.Pro109=
ENST00000634680.1:c.152-100T>C ENSP00000489240.1:n.152-100T>C
ENST00000634967.1:c.224-100T>C ENSP00000489559.1:n.224-100T>C
NR_074079.1:n.645-100T>C
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