Canonical Allele Identifier: CA405756289

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738428G>C (hg19) ; chr19:g.39247788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247788G>C , CM000681.2:g.39247788G>C	GRCh38
NC_000019.9:g.39738428G>C , CM000681.1:g.39738428G>C	GRCh37
NC_000019.8:g.44430268G>C	NCBI36
NG_042193.1:g.2184C>G
NG_055295.1:g.6069C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.287C>G	ENSP00000476098.1:p.Pro96Arg
ENST00000610963.1:c.286C>G	ENSP00000481371.1:p.Leu96Val
ENST00000616270.4:c.224-122C>G	ENSP00000480679.1:n.224-122C>G
ENST00000634680.1:c.152-325C>G	ENSP00000489240.1:n.152-325C>G
ENST00000634967.1:c.223+136C>G	ENSP00000489559.1:n.223+136C>G
NR_074079.1:n.564C>G