Canonical Allele Identifier: CA2576778289

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247686-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247686G>A , CM000681.2:g.39247686G>A	GRCh38
NC_000019.9:g.39738326G>A , CM000681.1:g.39738326G>A	GRCh37
NC_000019.8:g.44430166G>A	NCBI36
NG_042193.1:g.2286C>T
NG_055295.1:g.6171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+22C>T	ENSP00000476098.1:n.367+22C>T
ENST00000610963.1:c.366+22C>T	ENSP00000481371.1:n.366+22C>T
ENST00000616270.4:c.224-20C>T	ENSP00000480679.1:n.224-20C>T
ENST00000634680.1:c.152-223C>T	ENSP00000489240.1:n.152-223C>T
ENST00000634967.1:c.224-223C>T	ENSP00000489559.1:n.224-223C>T
NR_074079.1:n.644+22C>T