Canonical Allele Identifier: CA308189233
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs373966506
gnomAD v4: 19-39247687-C-T
MyVariant Identifiers: chr19:g.39738327C>T (hg19) chr19:g.39247687C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247687C>T , CM000681.2:g.39247687C>T GRCh38
NC_000019.9:g.39738327C>T , CM000681.1:g.39738327C>T GRCh37
NC_000019.8:g.44430167C>T NCBI36
NG_042193.1:g.2285G>A
NG_055295.1:g.6170G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+21G>A ENSP00000476098.1:n.367+21G>A
ENST00000610963.1:c.366+21G>A ENSP00000481371.1:n.366+21G>A
ENST00000616270.4:c.224-21G>A ENSP00000480679.1:n.224-21G>A
ENST00000634680.1:c.152-224G>A ENSP00000489240.1:n.152-224G>A
ENST00000634967.1:c.224-224G>A ENSP00000489559.1:n.224-224G>A
NR_074079.1:n.644+21G>A
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