Canonical Allele Identifier: CA507655487

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247449-C-G
• MyVariant Identifiers: chr19:g.39738089C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247449C>G , CM000681.2:g.39247449C>G	GRCh38
NC_000019.9:g.39738089C>G , CM000681.1:g.39738089C>G	GRCh37
NC_000019.8:g.44429929C>G	NCBI36
NG_042193.1:g.2523G>C
NG_055295.1:g.6408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.382G>C	ENSP00000476098.1:p.Ala128Pro
ENST00000610963.1:c.381G>C	ENSP00000481371.1:p.Arg127=
ENST00000616270.4:c.422+19G>C	ENSP00000480679.1:n.422+19G>C
ENST00000634680.1:c.166G>C	ENSP00000489240.1:p.Ala56Pro
ENST00000634967.1:c.238G>C	ENSP00000489559.1:p.Ala80Pro
NR_074079.1:n.659G>C