Canonical Allele Identifier: CA507407448

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247717-C-T
• MyVariant Identifiers: chr19:g.39738357C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247717C>T , CM000681.2:g.39247717C>T	GRCh38
NC_000019.9:g.39738357C>T , CM000681.1:g.39738357C>T	GRCh37
NC_000019.8:g.44430197C>T	NCBI36
NG_042193.1:g.2255G>A
NG_055295.1:g.6140G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.358G>A	ENSP00000476098.1:p.Gly120Ser
ENST00000610963.1:c.357G>A	ENSP00000481371.1:p.Val119=
ENST00000616270.4:c.224-51G>A	ENSP00000480679.1:n.224-51G>A
ENST00000634680.1:c.152-254G>A	ENSP00000489240.1:n.152-254G>A
ENST00000634967.1:c.223+207G>A	ENSP00000489559.1:n.223+207G>A
NR_074079.1:n.635G>A