Canonical Allele Identifier: CA308189033

Gene: IFNL4

Linked Data

• dbSNP Id: rs1013241354
• gnomAD v3: 19-39247528-T-A
• gnomAD v4: 19-39247528-T-A
• MyVariant Identifiers: chr19:g.39738168T>A (hg19) ; chr19:g.39247528T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247528T>A , CM000681.2:g.39247528T>A	GRCh38
NC_000019.9:g.39738168T>A , CM000681.1:g.39738168T>A	GRCh37
NC_000019.8:g.44430008T>A	NCBI36
NG_042193.1:g.2444A>T
NG_055295.1:g.6329A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-65A>T	ENSP00000476098.1:n.368-65A>T
ENST00000610963.1:c.367-65A>T	ENSP00000481371.1:n.367-65A>T
ENST00000616270.4:c.362A>T	ENSP00000480679.1:p.His121Leu
ENST00000634680.1:c.152-65A>T	ENSP00000489240.1:n.152-65A>T
ENST00000634967.1:c.224-65A>T	ENSP00000489559.1:n.224-65A>T
NR_074079.1:n.645-65A>T