Canonical Allele Identifier: CA9426139
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs111531283
ExAC: 19:39738317 A / C
gnomAD v2: 19-39738317-A-C
gnomAD v3: 19-39247677-A-C
gnomAD v4: 19-39247677-A-C
MyVariant Identifiers: chr19:g.39738317A>C (hg19) chr19:g.39247677A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247677A>C , CM000681.2:g.39247677A>C GRCh38
NC_000019.9:g.39738317A>C , CM000681.1:g.39738317A>C GRCh37
NC_000019.8:g.44430157A>C NCBI36
NG_042193.1:g.2295T>G
NG_055295.1:g.6180T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+31T>G ENSP00000476098.1:n.367+31T>G
ENST00000610963.1:c.366+31T>G ENSP00000481371.1:n.366+31T>G
ENST00000616270.4:c.224-11T>G ENSP00000480679.1:n.224-11T>G
ENST00000634680.1:c.152-214T>G ENSP00000489240.1:n.152-214T>G
ENST00000634967.1:c.224-214T>G ENSP00000489559.1:n.224-214T>G
NR_074079.1:n.644+31T>G
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