Canonical Allele Identifier: CA308189062

Gene: IFNL4

Linked Data

• dbSNP Id: rs1005945581
• MyVariant Identifiers: chr19:g.39738210C>T (hg19) ; chr19:g.39247570C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247570C>T , CM000681.2:g.39247570C>T	GRCh38
NC_000019.9:g.39738210C>T , CM000681.1:g.39738210C>T	GRCh37
NC_000019.8:g.44430050C>T	NCBI36
NG_042193.1:g.2402G>A
NG_055295.1:g.6287G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-107G>A	ENSP00000476098.1:n.368-107G>A
ENST00000610963.1:c.367-107G>A	ENSP00000481371.1:n.367-107G>A
ENST00000616270.4:c.320G>A	ENSP00000480679.1:p.Gly107Glu
ENST00000634680.1:c.152-107G>A	ENSP00000489240.1:n.152-107G>A
ENST00000634967.1:c.224-107G>A	ENSP00000489559.1:n.224-107G>A
NR_074079.1:n.645-107G>A