Canonical Allele Identifier: CA507655495

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247455-C-A
• MyVariant Identifiers: chr19:g.39738095C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247455C>A , CM000681.2:g.39247455C>A	GRCh38
NC_000019.9:g.39738095C>A , CM000681.1:g.39738095C>A	GRCh37
NC_000019.8:g.44429935C>A	NCBI36
NG_042193.1:g.2517G>T
NG_055295.1:g.6402G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.376G>T	ENSP00000476098.1:p.Gly126Cys
ENST00000610963.1:c.375G>T	ENSP00000481371.1:p.Leu125=
ENST00000616270.4:c.422+13G>T	ENSP00000480679.1:n.422+13G>T
ENST00000634680.1:c.160G>T	ENSP00000489240.1:p.Gly54Cys
ENST00000634967.1:c.232G>T	ENSP00000489559.1:p.Gly78Cys
NR_074079.1:n.653G>T