Canonical Allele Identifier: CA405755708

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247612-C-A
• MyVariant Identifiers: chr19:g.39738252C>A (hg19) ; chr19:g.39247612C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247612C>A , CM000681.2:g.39247612C>A	GRCh38
NC_000019.9:g.39738252C>A , CM000681.1:g.39738252C>A	GRCh37
NC_000019.8:g.44430092C>A	NCBI36
NG_042193.1:g.2360G>T
NG_055295.1:g.6245G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+96G>T	ENSP00000476098.1:n.367+96G>T
ENST00000610963.1:c.366+96G>T	ENSP00000481371.1:n.366+96G>T
ENST00000616270.4:c.278G>T	ENSP00000480679.1:p.Cys93Phe
ENST00000634680.1:c.152-149G>T	ENSP00000489240.1:n.152-149G>T
ENST00000634967.1:c.224-149G>T	ENSP00000489559.1:n.224-149G>T
NR_074079.1:n.644+96G>T