Canonical Allele Identifier: CA507655482

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247446-T-C
• MyVariant Identifiers: chr19:g.39738086T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247446T>C , CM000681.2:g.39247446T>C	GRCh38
NC_000019.9:g.39738086T>C , CM000681.1:g.39738086T>C	GRCh37
NC_000019.8:g.44429926T>C	NCBI36
NG_042193.1:g.2526A>G
NG_055295.1:g.6411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.385A>G	ENSP00000476098.1:p.Arg129Gly
ENST00000610963.1:c.384A>G	ENSP00000481371.1:p.Pro128=
ENST00000616270.4:c.422+22A>G	ENSP00000480679.1:n.422+22A>G
ENST00000634680.1:c.169A>G	ENSP00000489240.1:p.Arg57Gly
ENST00000634967.1:c.241A>G	ENSP00000489559.1:p.Arg81Gly
NR_074079.1:n.662A>G