Canonical Allele Identifier: CA405754966

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074954093
• gnomAD v4: 19-39247439-A-G
• MyVariant Identifiers: chr19:g.39738079A>G (hg19) ; chr19:g.39247439A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247439A>G , CM000681.2:g.39247439A>G	GRCh38
NC_000019.9:g.39738079A>G , CM000681.1:g.39738079A>G	GRCh37
NC_000019.8:g.44429919A>G	NCBI36
NG_042193.1:g.2533T>C
NG_055295.1:g.6418T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.392T>C	ENSP00000476098.1:p.Leu131Pro
ENST00000610963.1:c.391T>C	ENSP00000481371.1:p.Ser131Pro
ENST00000616270.4:c.422+29T>C	ENSP00000480679.1:n.422+29T>C
ENST00000634680.1:c.176T>C	ENSP00000489240.1:p.Leu59Pro
ENST00000634967.1:c.248T>C	ENSP00000489559.1:p.Leu83Pro
NR_074079.1:n.669T>C