Canonical Allele Identifier: CA405756512
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247844-G-T
MyVariant Identifiers: chr19:g.39738484G>T (hg19) chr19:g.39247844G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247844G>T , CM000681.2:g.39247844G>T GRCh38
NC_000019.9:g.39738484G>T , CM000681.1:g.39738484G>T GRCh37
NC_000019.8:g.44430324G>T NCBI36
NG_042193.1:g.2128C>A
NG_055295.1:g.6013C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.231C>A ENSP00000476098.1:p.Arg77=
ENST00000610963.1:c.230C>A ENSP00000481371.1:p.Ala77Asp
ENST00000616270.4:c.223+80C>A ENSP00000480679.1:n.223+80C>A
ENST00000634680.1:c.152-381C>A ENSP00000489240.1:n.152-381C>A
ENST00000634967.1:c.223+80C>A ENSP00000489559.1:n.223+80C>A
NR_074079.1:n.508C>A
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