Canonical Allele Identifier: CA405756549
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247852-C-T
MyVariant Identifiers: chr19:g.39738492C>T (hg19) chr19:g.39247852C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247852C>T , CM000681.2:g.39247852C>T GRCh38
NC_000019.9:g.39738492C>T , CM000681.1:g.39738492C>T GRCh37
NC_000019.8:g.44430332C>T NCBI36
NG_042193.1:g.2120G>A
NG_055295.1:g.6005G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.224-1G>A ENSP00000476098.1:n.224-1G>A
ENST00000610963.1:c.223-1G>A ENSP00000481371.1:n.223-1G>A
ENST00000616270.4:c.223+72G>A ENSP00000480679.1:n.223+72G>A
ENST00000634680.1:c.152-389G>A ENSP00000489240.1:n.152-389G>A
ENST00000634967.1:c.223+72G>A ENSP00000489559.1:n.223+72G>A
NR_074079.1:n.501-1G>A
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