ClinGen Allele Registry
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Canonical Allele Identifier:
CA507407521
Gene: IFNL4
HGNC
NCBI
Linked Data
dbSNP Id:
rs2074955774
gnomAD v4:
19-39247741-C-T
MyVariant Identifiers:
chr19:g.39738381C>T (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247741C>T , CM000681.2:g.39247741C>T
GRCh38
NC_000019.9:g.39738381C>T , CM000681.1:g.39738381C>T
GRCh37
NC_000019.8:g.44430221C>T
NCBI36
NG_042193.1:g.2231G>A
NG_055295.1:g.6116G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000606380.2:c.334G>A
ENSP00000476098.1:p.Ala112Thr
ENST00000610963.1:c.333G>A
ENSP00000481371.1:p.Leu111=
ENST00000616270.4:c.224-75G>A
ENSP00000480679.1:n.224-75G>A
ENST00000634680.1:c.152-278G>A
ENSP00000489240.1:n.152-278G>A
ENST00000634967.1:c.223+183G>A
ENSP00000489559.1:n.223+183G>A
NR_074079.1:n.611G>A
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