Canonical Allele Identifier: CA995767383
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs546893122
gnomAD v3: 19-39247902-C-G
gnomAD v4: 19-39247902-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247902C>G , CM000681.2:g.39247902C>G GRCh38
NC_000019.9:g.39738542C>G , CM000681.1:g.39738542C>G GRCh37
NC_000019.8:g.44430382C>G NCBI36
NG_042193.1:g.2070G>C
NG_055295.1:g.5955G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.223+22G>C ENSP00000476098.1:n.223+22G>C
ENST00000610963.1:c.222+22G>C ENSP00000481371.1:n.222+22G>C
ENST00000616270.4:c.223+22G>C ENSP00000480679.1:n.223+22G>C
ENST00000634680.1:c.152-439G>C ENSP00000489240.1:n.152-439G>C
ENST00000634967.1:c.223+22G>C ENSP00000489559.1:n.223+22G>C
NR_074079.1:n.500+22G>C
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