Canonical Allele Identifier: CA308189871
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs963204633
gnomAD v2: 19-39738998-A-G
gnomAD v3: 19-39248358-A-G
gnomAD v4: 19-39248358-A-G
MyVariant Identifiers: chr19:g.39738998A>G (hg19) chr19:g.39248358A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248358A>G , CM000681.2:g.39248358A>G GRCh38
NC_000019.9:g.39738998A>G , CM000681.1:g.39738998A>G GRCh37
NC_000019.8:g.44430838A>G NCBI36
NG_042193.1:g.1614T>C
NG_055295.1:g.5499T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+71T>C ENSP00000476098.1:n.151+71T>C
ENST00000610963.1:c.150+71T>C ENSP00000481371.1:n.150+71T>C
ENST00000616270.4:c.151+71T>C ENSP00000480679.1:n.151+71T>C
ENST00000634680.1:c.151+71T>C ENSP00000489240.1:n.151+71T>C
ENST00000634967.1:c.151+71T>C ENSP00000489559.1:n.151+71T>C
NR_074079.1:n.428+71T>C
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