Canonical Allele Identifier: CA507407565

Gene: IFNL4

Linked Data

• dbSNP Id: rs941739023
• gnomAD v3: 19-39247780-G-A
• gnomAD v4: 19-39247780-G-A
• MyVariant Identifiers: chr19:g.39738420G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247780G>A , CM000681.2:g.39247780G>A	GRCh38
NC_000019.9:g.39738420G>A , CM000681.1:g.39738420G>A	GRCh37
NC_000019.8:g.44430260G>A	NCBI36
NG_042193.1:g.2192C>T
NG_055295.1:g.6077C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.295C>T	ENSP00000476098.1:p.Leu99Phe
ENST00000610963.1:c.294C>T	ENSP00000481371.1:p.Arg98=
ENST00000616270.4:c.224-114C>T	ENSP00000480679.1:n.224-114C>T
ENST00000634680.1:c.152-317C>T	ENSP00000489240.1:n.152-317C>T
ENST00000634967.1:c.223+144C>T	ENSP00000489559.1:n.223+144C>T
NR_074079.1:n.572C>T