Canonical Allele Identifier: CA405756000

Gene: IFNL4

Linked Data

• dbSNP Id: rs1404097226
• gnomAD v3: 19-39247715-G-A
• gnomAD v4: 19-39247715-G-A
• MyVariant Identifiers: chr19:g.39738355G>A (hg19) ; chr19:g.39247715G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247715G>A , CM000681.2:g.39247715G>A	GRCh38
NC_000019.9:g.39738355G>A , CM000681.1:g.39738355G>A	GRCh37
NC_000019.8:g.44430195G>A	NCBI36
NG_042193.1:g.2257C>T
NG_055295.1:g.6142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.360C>T	ENSP00000476098.1:p.Gly120=
ENST00000610963.1:c.359C>T	ENSP00000481371.1:p.Ala120Val
ENST00000616270.4:c.224-49C>T	ENSP00000480679.1:n.224-49C>T
ENST00000634680.1:c.152-252C>T	ENSP00000489240.1:n.152-252C>T
ENST00000634967.1:c.223+209C>T	ENSP00000489559.1:n.223+209C>T
NR_074079.1:n.637C>T