Canonical Allele Identifier: CA405755067
Gene: IFNL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39738105T>A (hg19) chr19:g.39247465T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247465T>A , CM000681.2:g.39247465T>A GRCh38
NC_000019.9:g.39738105T>A , CM000681.1:g.39738105T>A GRCh37
NC_000019.8:g.44429945T>A NCBI36
NG_042193.1:g.2507A>T
NG_055295.1:g.6392A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.368-2A>T ENSP00000476098.1:n.368-2A>T
ENST00000610963.1:c.367-2A>T ENSP00000481371.1:n.367-2A>T
ENST00000616270.4:c.422+3A>T ENSP00000480679.1:n.422+3A>T
ENST00000634680.1:c.152-2A>T ENSP00000489240.1:n.152-2A>T
ENST00000634967.1:c.224-2A>T ENSP00000489559.1:n.224-2A>T
NR_074079.1:n.645-2A>T
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