Canonical Allele Identifier: CA405755292

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247514-T-C
• MyVariant Identifiers: chr19:g.39738154T>C (hg19) ; chr19:g.39247514T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247514T>C , CM000681.2:g.39247514T>C	GRCh38
NC_000019.9:g.39738154T>C , CM000681.1:g.39738154T>C	GRCh37
NC_000019.8:g.44429994T>C	NCBI36
NG_042193.1:g.2458A>G
NG_055295.1:g.6343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-51A>G	ENSP00000476098.1:n.368-51A>G
ENST00000610963.1:c.367-51A>G	ENSP00000481371.1:n.367-51A>G
ENST00000616270.4:c.376A>G	ENSP00000480679.1:p.Arg126Gly
ENST00000634680.1:c.152-51A>G	ENSP00000489240.1:n.152-51A>G
ENST00000634967.1:c.224-51A>G	ENSP00000489559.1:n.224-51A>G
NR_074079.1:n.645-51A>G