Canonical Allele Identifier: CA2584994692

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247638-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247638C>T , CM000681.2:g.39247638C>T	GRCh38
NC_000019.9:g.39738278C>T , CM000681.1:g.39738278C>T	GRCh37
NC_000019.8:g.44430118C>T	NCBI36
NG_042193.1:g.2334G>A
NG_055295.1:g.6219G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+70G>A	ENSP00000476098.1:n.367+70G>A
ENST00000610963.1:c.366+70G>A	ENSP00000481371.1:n.366+70G>A
ENST00000616270.4:c.252G>A	ENSP00000480679.1:p.Glu84=
ENST00000634680.1:c.152-175G>A	ENSP00000489240.1:n.152-175G>A
ENST00000634967.1:c.224-175G>A	ENSP00000489559.1:n.224-175G>A
NR_074079.1:n.644+70G>A