Canonical Allele Identifier: CA507655498

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247457-G-A
• MyVariant Identifiers: chr19:g.39738097G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247457G>A , CM000681.2:g.39247457G>A	GRCh38
NC_000019.9:g.39738097G>A , CM000681.1:g.39738097G>A	GRCh37
NC_000019.8:g.44429937G>A	NCBI36
NG_042193.1:g.2515C>T
NG_055295.1:g.6400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.374C>T	ENSP00000476098.1:p.Ala125Val
ENST00000610963.1:c.373C>T	ENSP00000481371.1:p.Leu125=
ENST00000616270.4:c.422+11C>T	ENSP00000480679.1:n.422+11C>T
ENST00000634680.1:c.158C>T	ENSP00000489240.1:p.Ala53Val
ENST00000634967.1:c.230C>T	ENSP00000489559.1:p.Ala77Val
NR_074079.1:n.651C>T