Canonical Allele Identifier: CA405755701

Gene: IFNL4

Linked Data

• dbSNP Id: rs1208788472
• gnomAD v2: 19-39738250-A-C
• gnomAD v3: 19-39247610-A-C
• gnomAD v4: 19-39247610-A-C
• MyVariant Identifiers: chr19:g.39738250A>C (hg19) ; chr19:g.39247610A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247610A>C , CM000681.2:g.39247610A>C	GRCh38
NC_000019.9:g.39738250A>C , CM000681.1:g.39738250A>C	GRCh37
NC_000019.8:g.44430090A>C	NCBI36
NG_042193.1:g.2362T>G
NG_055295.1:g.6247T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+98T>G	ENSP00000476098.1:n.367+98T>G
ENST00000610963.1:c.366+98T>G	ENSP00000481371.1:n.366+98T>G
ENST00000616270.4:c.280T>G	ENSP00000480679.1:p.Leu94Val
ENST00000634680.1:c.152-147T>G	ENSP00000489240.1:n.152-147T>G
ENST00000634967.1:c.224-147T>G	ENSP00000489559.1:n.224-147T>G
NR_074079.1:n.644+98T>G