Canonical Allele Identifier: CA405755178

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247489-G-A
• MyVariant Identifiers: chr19:g.39738129G>A (hg19) ; chr19:g.39247489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247489G>A , CM000681.2:g.39247489G>A	GRCh38
NC_000019.9:g.39738129G>A , CM000681.1:g.39738129G>A	GRCh37
NC_000019.8:g.44429969G>A	NCBI36
NG_042193.1:g.2483C>T
NG_055295.1:g.6368C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-26C>T	ENSP00000476098.1:n.368-26C>T
ENST00000610963.1:c.367-26C>T	ENSP00000481371.1:n.367-26C>T
ENST00000616270.4:c.401C>T	ENSP00000480679.1:p.Ser134Phe
ENST00000634680.1:c.152-26C>T	ENSP00000489240.1:n.152-26C>T
ENST00000634967.1:c.224-26C>T	ENSP00000489559.1:n.224-26C>T
NR_074079.1:n.645-26C>T