Canonical Allele Identifier: CA405755469

Gene: IFNL4

Linked Data

• dbSNP Id: rs1388609153
• gnomAD v2: 19-39738195-C-T
• gnomAD v3: 19-39247555-C-T
• gnomAD v4: 19-39247555-C-T
• MyVariant Identifiers: chr19:g.39738195C>T (hg19) ; chr19:g.39247555C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247555C>T , CM000681.2:g.39247555C>T	GRCh38
NC_000019.9:g.39738195C>T , CM000681.1:g.39738195C>T	GRCh37
NC_000019.8:g.44430035C>T	NCBI36
NG_042193.1:g.2417G>A
NG_055295.1:g.6302G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-92G>A	ENSP00000476098.1:n.368-92G>A
ENST00000610963.1:c.367-92G>A	ENSP00000481371.1:n.367-92G>A
ENST00000616270.4:c.335G>A	ENSP00000480679.1:p.Arg112Gln
ENST00000634680.1:c.152-92G>A	ENSP00000489240.1:n.152-92G>A
ENST00000634967.1:c.224-92G>A	ENSP00000489559.1:n.224-92G>A
NR_074079.1:n.645-92G>A