Canonical Allele Identifier: CA405755590

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247586-C-A
• MyVariant Identifiers: chr19:g.39738226C>A (hg19) ; chr19:g.39247586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247586C>A , CM000681.2:g.39247586C>A	GRCh38
NC_000019.9:g.39738226C>A , CM000681.1:g.39738226C>A	GRCh37
NC_000019.8:g.44430066C>A	NCBI36
NG_042193.1:g.2386G>T
NG_055295.1:g.6271G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-123G>T	ENSP00000476098.1:n.368-123G>T
ENST00000610963.1:c.367-123G>T	ENSP00000481371.1:n.367-123G>T
ENST00000616270.4:c.304G>T	ENSP00000480679.1:p.Gly102Ter
ENST00000634680.1:c.152-123G>T	ENSP00000489240.1:n.152-123G>T
ENST00000634967.1:c.224-123G>T	ENSP00000489559.1:n.224-123G>T
NR_074079.1:n.645-123G>T