Canonical Allele Identifier: CA405755781

Gene: IFNL4

Linked Data

• dbSNP Id: rs1318500794
• gnomAD v3: 19-39247628-A-G
• gnomAD v4: 19-39247628-A-G
• MyVariant Identifiers: chr19:g.39738268A>G (hg19) ; chr19:g.39247628A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247628A>G , CM000681.2:g.39247628A>G	GRCh38
NC_000019.9:g.39738268A>G , CM000681.1:g.39738268A>G	GRCh37
NC_000019.8:g.44430108A>G	NCBI36
NG_042193.1:g.2344T>C
NG_055295.1:g.6229T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+80T>C	ENSP00000476098.1:n.367+80T>C
ENST00000610963.1:c.366+80T>C	ENSP00000481371.1:n.366+80T>C
ENST00000616270.4:c.262T>C	ENSP00000480679.1:p.Phe88Leu
ENST00000634680.1:c.152-165T>C	ENSP00000489240.1:n.152-165T>C
ENST00000634967.1:c.224-165T>C	ENSP00000489559.1:n.224-165T>C
NR_074079.1:n.644+80T>C