Canonical Allele Identifier: CA2584994807
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247914-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247914C>G , CM000681.2:g.39247914C>G GRCh38
NC_000019.9:g.39738554C>G , CM000681.1:g.39738554C>G GRCh37
NC_000019.8:g.44430394C>G NCBI36
NG_042193.1:g.2058G>C
NG_055295.1:g.5943G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.223+10G>C ENSP00000476098.1:n.223+10G>C
ENST00000610963.1:c.222+10G>C ENSP00000481371.1:n.222+10G>C
ENST00000616270.4:c.223+10G>C ENSP00000480679.1:n.223+10G>C
ENST00000634680.1:c.152-451G>C ENSP00000489240.1:n.152-451G>C
ENST00000634967.1:c.223+10G>C ENSP00000489559.1:n.223+10G>C
NR_074079.1:n.500+10G>C
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