Canonical Allele Identifier: CA2584994668

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247530-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247530G>T , CM000681.2:g.39247530G>T	GRCh38
NC_000019.9:g.39738170G>T , CM000681.1:g.39738170G>T	GRCh37
NC_000019.8:g.44430010G>T	NCBI36
NG_042193.1:g.2442C>A
NG_055295.1:g.6327C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-67C>A	ENSP00000476098.1:n.368-67C>A
ENST00000610963.1:c.367-67C>A	ENSP00000481371.1:n.367-67C>A
ENST00000616270.4:c.360C>A	ENSP00000480679.1:p.Gly120=
ENST00000634680.1:c.152-67C>A	ENSP00000489240.1:n.152-67C>A
ENST00000634967.1:c.224-67C>A	ENSP00000489559.1:n.224-67C>A
NR_074079.1:n.645-67C>A